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 13:102856110 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM016233

Most severe consequence
Clinical significance

Synonyms

LSDB 1783

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

13:g.102856110C>T
ENST00000602836.1:c.1802C>T
ENSP00000473384.1:p.Gln602Ter
ENST00000535557.3:c.526C>T
ENSP00000442117.1:p.Gln176Ter
ENST00000355739.6:c.526C>T
ENSP00000347978.4:p.Gln176Ter
ENST00000610537.2:c.526C>T
ENSP00000478667.1:p.Gln176Ter
LRG_464:g.15287C>T
LRG_464t1:c.526C>T
LRG_464p1:p.Gln176Ter

Variation displays