Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 15:38351113 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM093925

Most severe consequence
Clinical significance

Synonyms

LSDB 16211

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

15:g.38351113A>T
ENST00000299084.6:c.784A>T
ENSP00000299084.4:p.Arg262Ter

Variation displays