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 12:25227341 (forward strand) | View in location tab

Co-located

with COSMIC COSM555 (T/A), COSM554 (T/G), COSM1135364 (T/G), COSM1146992 (T/A)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2 sample genotypes and is associated with 3 phenotypes.

Variant displays