Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 10:71785051 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM057323

Most severe consequence
Clinical significance

Synonyms

LSDB 13252

This variation has 5 HGVS names - click the plus to show

10:g.71785051T>C
ENST00000622827.1:c.5663T>C
ENSP00000483211.1:p.Phe1888Ser
ENST00000224721.7:c.5813T>C
ENSP00000224721.7:p.Phe1938Ser

Variation displays