Original source

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

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

Chromosome 10:71812822 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM050001

Most severe consequence
Clinical significance

Synonyms

LSDB 13254

This variation has 10 HGVS names - click the plus to show

10:g.71812822C>T
ENST00000622827.1:c.9565C>T
ENSP00000483211.1:p.Arg3189Trp
ENST00000619887.1:c.2845C>T
ENSP00000478374.1:p.Arg949Trp
ENST00000398788.4:c.2845C>T
ENSP00000381768.3:p.Arg949Trp
ENST00000224721.7:c.9715C>T
ENSP00000224721.7:p.Arg3239Trp
ENST00000475158.1:n.3101C>T

Variation displays