Original source

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

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

Chromosome 7:55191822 (forward strand) | View in location tab

Co-located

with COSMIC COSM6224 (T/G), COSM29578 (T/A)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature and is associated with 4 phenotypes.

Variant displays