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 22:37723595 (forward strand) | View in location tab

Co-located

with COSMIC COSM1034038 (C/T) ; HGMD-PUBLIC CM067723

Most severe consequence
Clinical significance

Synonyms

LSDB 16515

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

22:g.37723595C>T
ENST00000455236.3:c.*1375C>T
ENST00000406386.4:c.1039C>T
ENSP00000384312.3:p.Arg347Ter
ENST00000344404.7:c.*522C>T
ENST00000492485.2:n.973C>T

Variation displays