Original source

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

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

Chromosome 7:55191831 (forward strand) | View in location tab

Co-located

with COSMIC COSM6213 (T/A), COSM12374 (T/G)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays