Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 15:66436837 (forward strand) | View in location tab

Co-located

with COSMIC COSM1374186 (G/A), COSM1517232 (G/T) ; HGMD-PUBLIC CM080433

Most severe consequence
Clinical significance

Synonyms

LSDB 4945

This variation has 7 HGVS names - click the plus to show

15:g.66436837G>T
ENST00000425818.2:n.894G>T
ENST00000307102.7:c.383G>T
ENSP00000302486.4:p.Gly128Val
LRG_725:g.54965G>T
LRG_725t1:c.383G>T
LRG_725p1:p.Gly128Val

Variation displays