Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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


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

Most severe consequence

This variation has 3 synonyms - click the plus to show

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

About this variant

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

Variation displays