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 22:37725905 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM060498

Most severe consequence
Clinical significance

Synonyms

LSDB 16520

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

22:g.37725905C>T
ENST00000455236.3:c.*3685C>T
ENST00000406386.5:c.3349C>T
ENSP00000384312.3:p.Arg1117Ter
ENST00000344404.8:c.*2832C>T
ENST00000492485.3:n.3283C>T

Variation displays