Original source

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

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

Chromosome 10:73572579 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM050001

Most severe consequence
Clinical significance

Synonyms

LSDB 13254

This variation has 6 HGVS names - click the plus to show

10:g.73572579C>T
ENST00000398788.3:c.2845C>T
ENSP00000381768.3:p.Arg949Trp
ENST00000224721.6:c.9580C>T
ENSP00000224721.6:p.Arg3194Trp
ENST00000475158.1:n.3101C>T

Variation displays