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 15:38641677 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM093930

Most severe consequence
Clinical significance

Synonyms

LSDB 16210

This variation has 3 HGVS names - click the plus to show

15:g.38641677C>T
ENST00000299084.4:c.637C>T
ENSP00000299084.4:p.Gln213Ter

Variation displays