{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HGNC:644,10,HGNC:644,13,4]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:644","source":"HGNC:644|androgen receptor","targets":["1177442|NM_000044.6(AR):c.2255G>C (p.Trp752Ser)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1207735|NM_000044.6(AR):c.2450-42G>A|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1298366|NM_000044.6(AR):c.1742A>C (p.Lys581Thr)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1323926|NM_000044.6(AR):c.649del (p.Ala217fs)|Deletion|Likely pathogenic|AR|criteria provided, single submitter|X","1338633|NM_000044.6(AR):c.2668G>T (p.Val890Leu)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1480317|NM_000044.6(AR):c.2318A>G (p.Glu773Gly)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1506100|NM_000044.6(AR):c.2126G>T (p.Gly709Val)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1677702|NM_000044.6(AR):c.1395_1426del (p.Gly466fs)|Deletion|Likely pathogenic|AR|criteria provided, single submitter|X","1687577|NM_000044.6(AR):c.1768+1G>A|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1698951|NM_000044.6(AR):c.2076C>A (p.Asn692Lys)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1699192|NM_000044.6(AR):c.2056G>C (p.Val686Leu)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1705334|NM_000044.6(AR):c.1181_1200dup (p.Ala401fs)|Duplication|Likely pathogenic|AR|criteria provided, single submitter|X","1705712|NM_000044.6(AR):c.1933G>T (p.Glu645Ter)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1713192|NM_000044.6(AR):c.1737C>A (p.Ser579Arg)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1727214|NM_000044.6(AR):c.1396_1397insAG (p.Gly466fs)|Insertion|Likely pathogenic|AR|no assertion criteria provided|X","1805862|NM_000044.6(AR):c.1749C>G (p.Phe583Leu)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1918318|NM_000044.6(AR):c.2761T>C (p.Ter921Arg)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2000750|NM_000044.6(AR):c.2174-2A>G|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2138585|NM_000044.6(AR):c.2087A>T (p.Asp696Val)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2138590|NM_000044.6(AR):c.2710G>A (p.Val904Met)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","219296|NM_000044.6(AR):c.2105T>A (p.Leu702His)|single nucleotide variant|Likely pathogenic|AR|no assertion criteria provided|X","2431800|NM_000044.6(AR):c.2221T>C (p.Ser741Pro)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2445341|NM_000044.6(AR):c.1976A>G (p.Lys659Arg)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2445359|NM_000044.6(AR):c.1421A>G (p.Glu474Gly)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2445360|NM_000044.6(AR):c.1157G>T (p.Arg386Leu)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2445373|NM_000044.6(AR):c.2207C>A (p.Ala736Asp)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2445393|NM_000044.6(AR):c.1360G>A (p.Gly454Arg)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2502891|NM_000044.6(AR):c.2636T>C (p.Phe879Ser)|single nucleotide variant|Likely pathogenic|AR|no assertion criteria provided|X","2507021|NM_000044.6(AR):c.2317G>A (p.Glu773Lys)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2573824|NM_000044.6(AR):c.1787G>A (p.Cys596Tyr)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2573828|NM_000044.6(AR):c.2344T>G (p.Tyr782Asp)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2575082|NM_000044.6(AR):c.2072A>G (p.Asp691Gly)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2630763|NM_000044.6(AR):c.1103del (p.Pro368fs)|Deletion|Likely pathogenic|AR|criteria provided, single submitter|X","2631223|NM_000044.6(AR):c.2473C>A (p.Gln825Lys)|single nucleotide variant|Likely pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","2674670|NM_000044.6(AR):c.1341T>A (p.Tyr447Ter)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2674671|NM_000044.6(AR):c.2339G>C (p.Arg780Pro)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2674672|NM_000044.6(AR):c.2449+1_2449+3dup|Duplication|Likely pathogenic|AR|criteria provided, single submitter|X","268093|NM_000044.6(AR):c.1685T>C (p.Ile562Thr)|single nucleotide variant|Likely pathogenic|AR|no assertion criteria provided|X","2690958|NM_000044.6(AR):c.1286C>A (p.Ala429Asp)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2692296|NM_000044.6(AR):c.1616+1_1616+3delinsT|Indel|Likely pathogenic|AR|no assertion criteria provided|X","2925677|NM_000044.6(AR):c.2169G>T (p.Leu723Phe)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2925679|NM_000044.6(AR):c.2233C>T (p.Leu745Phe)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","2942787|NM_000044.6(AR):c.1743G>C (p.Lys581Asn)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3046291|NM_000044.6(AR):c.1616+1_1616+2dup|Duplication|Likely pathogenic|AR|no assertion criteria provided|X","3061773|NM_000044.6(AR):c.1852C>T (p.Arg618Trp)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3061775|NM_000044.6(AR):c.2360G>A (p.Arg787Gln)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3062241|NM_000044.6(AR):c.2449+1G>A|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3062254|NM_000044.6(AR):c.35del (p.Pro12fs)|Deletion|Likely pathogenic|AR|criteria provided, single submitter|X","3062281|NM_000044.6(AR):c.1873A>G (p.Met625Val)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3062325|NM_000044.6(AR):c.2079C>G (p.Asn693Lys)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3255195|NM_000044.6(AR):c.1835G>C (p.Cys612Ser)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3336685|NM_000044.6(AR):c.2287C>G (p.Leu763Val)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3336687|NM_000044.6(AR):c.2302G>T (p.Asp768Tyr)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3340138|NM_000044.6(AR):c.1421_1425dup (p.Gly476fs)|Duplication|Likely pathogenic|AR|no assertion criteria provided|X","3347404|NM_000044.6(AR):c.2673_2675dup (p.Phe892_Pro893insPhe)|Duplication|Likely pathogenic|AR|no assertion criteria provided|X","3353504|NM_000044.6(AR):c.-547C>T|single nucleotide variant|Likely pathogenic|AR|no assertion criteria provided|X","3362262|NM_000044.6(AR):c.2612C>G (p.Ala871Gly)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3367174|NM_000044.6(AR):c.2318+3_2318+6del|Deletion|Likely pathogenic|AR|no assertion criteria provided|X","3572937|NM_000044.6(AR):c.1828A>G (p.Lys610Glu)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3759645|NM_000044.6(AR):c.1757G>A (p.Arg586Lys)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3759647|NM_000044.6(AR):c.2046G>T (p.Glu682Asp)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3760521|NM_000044.6(AR):c.2714C>T (p.Pro905Leu)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3761867|NM_000044.6(AR):c.160_162dup (p.Leu57_Gln58insLeu)|Duplication|Likely pathogenic|AR|criteria provided, single submitter|X","3767296|NM_000044.6(AR):c.2246C>T (p.Ala749Val)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3775706|NM_000044.6(AR):c.2740C>T (p.Pro914Ser)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","381643|NM_000044.6(AR):c.1720G>C (p.Ala574Pro)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","3893234|NM_000044.6(AR):c.1769G>A (p.Gly590Glu)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","390372|NM_000044.6(AR):c.2258G>T (p.Arg753Leu)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","391803|NM_000044.6(AR):c.2137C>A (p.Leu713Ile)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4077404|NM_000044.6(AR):c.2045A>G (p.Glu682Gly)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4077405|NM_000044.6(AR):c.2545_2546delinsT (p.Asn849fs)|Indel|Likely pathogenic|AR|criteria provided, single submitter|X","4081595|NM_000044.6(AR):c.2329C>G (p.His777Asp)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4081597|NM_000044.6(AR):c.2567G>C (p.Arg856Pro)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4082473|NM_000044.6(AR):c.1742A>G (p.Lys581Arg)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4082475|NM_000044.6(AR):c.2131A>G (p.Arg711Gly)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4082479|NM_000044.6(AR):c.2432T>C (p.Leu811Pro)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","421614|NM_000044.6(AR):c.2740C>A (p.Pro914Thr)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","427107|NM_000044.6(AR):c.1888C>T (p.Arg630Trp)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4281683|NM_000044.6(AR):c.2700C>G (p.Ile900Met)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4281691|NM_000044.6(AR):c.2296G>T (p.Ala766Ser)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4293132|NM_000044.6(AR):c.235C>T (p.Gln79Ter)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4294427|NM_000044.6(AR):c.1786T>C (p.Cys596Arg)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4294499|NM_000044.6(AR):c.1218C>A (p.Cys406Ter)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","429930|NM_000044.6(AR):c.2723T>A (p.Leu908His)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","430163|NM_000044.6(AR):c.2668G>C (p.Val890Leu)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","434267|NM_000044.6(AR):c.2090C>A (p.Ser697Tyr)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","451908|NM_000044.6(AR):c.1813G>C (p.Asp605His)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4531344|NM_000044.6(AR):c.1750T>G (p.Phe584Val)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","4538399|NM_000044.6(AR):c.2492T>A (p.Leu831His)|single nucleotide variant|Likely pathogenic|AR|no assertion criteria provided|X","4538409|NM_000044.6(AR):c.2T>C (p.Met1Thr)|single nucleotide variant|Likely pathogenic|AR|no assertion criteria provided|X","4538438|NM_000044.6(AR):c.1753A>C (p.Lys585Gln)|single nucleotide variant|Likely pathogenic|AR|no assertion criteria provided|X","458359|NM_000044.6(AR):c.1805G>A (p.Cys602Tyr)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","458360|NM_000044.6(AR):c.1850T>C (p.Leu617Pro)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","458361|NM_000044.6(AR):c.2103G>T (p.Leu701Phe)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","464791|NM_000044.6(AR):c.1736G>C (p.Ser579Thr)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","464800|NM_000044.6(AR):c.2696T>C (p.Ile899Thr)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","464801|NM_000044.6(AR):c.2698A>T (p.Ile900Phe)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","492788|NM_000044.6(AR):c.2104C>T (p.Leu702Phe)|single nucleotide variant|Likely pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","533378|NM_000044.6(AR):c.2053G>A (p.Val685Ile)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","915284|NM_000044.6(AR):c.2342T>A (p.Met781Lys)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X"]}]}