Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 13:103508460 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 1783

This variation has 10 HGVS names - click the plus to show

13:g.103508460C>T
ENST00000602836.1:c.1802C>T
ENSP00000473384.1:p.Gln602Ter
ENST00000535557.1:c.526C>T
ENSP00000442117.1:p.Gln176Ter
ENST00000355739.4:c.526C>T
ENSP00000347978.4:p.Gln176Ter
LRG_464:g.15287C>T
LRG_464t1.1:c.526C>T
LRG_464p1.1:p.Gln176Ter

Variation displays