Original source

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

T/G | Ancestral: T | Ambiguity code: K

Chromosome 17:50185606 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, has 1 sample genotype and is mentioned in 1 citation.

Variant displays