This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/A/C/G | Ancestral: T | Ambiguity code: N

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


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

Most severe consequence
Stop gained
Evidence status


This variant has 3 synonyms - Show

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and is associated with 1 phenotype.

Variant displays