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 13:102854313 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 1790

This variation has 12 HGVS names - click the plus to show

13:g.102854313C>T
ENST00000602836.1:c.1682C>T
ENSP00000473384.1:p.Gln562Ter
ENST00000535557.2:c.406C>T
ENSP00000442117.1:p.Gln136Ter
ENST00000355739.5:c.406C>T
ENSP00000347978.4:p.Gln136Ter
ENST00000610537.1:c.406C>T
ENSP00000478667.1:p.Gln136Ter
LRG_464:g.13490C>T
LRG_464t1.1:c.406C>T
LRG_464p1.1:p.Gln136Ter

Variation displays