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 15:38299410 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM074578

Most severe consequence
Clinical significance

Synonyms

LSDB 16206

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

15:g.38299410C>T
ENST00000561317.1:c.7C>T
ENSP00000453680.1:p.Arg3Ter
ENST00000299084.6:c.70C>T
ENSP00000299084.4:p.Arg24Ter
ENST00000561205.1:n.408C>T

Variation displays