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 10:87952159 (forward strand) | View in location tab

Co-located

with COSMIC COSM28911 (T/A) ; HGMD-PUBLIC CM033669, CM013786, CX984035

Most severe consequence
 
Stop gained
Evidence status

This variant has 3 synonyms - click the plus to show

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

About this variant

This variant overlaps 6 transcripts and is associated with 1 phenotype.

Variant displays