Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 10:89711916 (forward strand) | View in location tab


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

Most severe consequence

This variation has 3 synonyms - click the plus to show

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

Variation displays