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AR c.1616+3A>C

rs1057518601 · VCV373772

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
Splice regiondonor +3donor splice region (+3, within the first 6 intronic nt) · inside the BP7-excluded zone
SpliceAI—not assessed · no allele here is in the release
PangolinΔ0.66loss · gain 0.01 · not in the SpliceAI release · independent
Constraint at this position
ConservationphyloP 6.8GERP 2.1, phastCons 1
Non-coding constraint—not assessed · autosomes only, so chrX has no window · absence ≠ unconstrained
Overall
CADD22.4PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene
AR
Coding
c.1616+3A>C
MANE Select
NM_000044
dbSNP
rs1057518601
Type
single nucleotide variant
Location
chrX:67546765 (GRCh38)
Structure
AlphaFold pLDDT 58.85 · 95 PDB
Full AR gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →

Cite Sugi Variant

Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/ar-c-1616-plus-3a-c (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown