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 13:102872397 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940377

Most severe consequence
Clinical significance

Synonyms

LSDB 1778

This variation has 11 HGVS names - click the plus to show

13:g.102872397G>T
ENST00000602836.1:c.4154G>T
ENST00000355739.5:c.2878G>T
ENSP00000347978.4:p.Glu960Ter
ENST00000610537.1:c.2875G>T
ENSP00000478667.1:p.Glu959Ter
ENST00000375954.1:c.577G>T
ENSP00000365121.1:p.Glu193Ter
LRG_464:g.31574G>T
LRG_464t1.1:c.2878G>T
LRG_464p1.1:p.Glu960Ter

Variation displays