Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 1:158685290 (forward strand) | View in location tab

Co-located

with COSMIC COSM1335249 (G/A) ; HGMD-PUBLIC CM910358, CM910359

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

This variant has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature and is associated with 6 phenotypes.

Variant displays