Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

C/A/T|Ancestral: C|Ambiguity code: H

Chromosome 17:7675088 (forward strand)|View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 5 synonyms - Show

HGVS names

This variant has 156 HGVS names - Show

About this variant

This variant overlaps 86 transcripts, is associated with 5 phenotypes and is mentioned in 4 citations.

Somatic mutation displays