Original source

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

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

Chromosome 13:102868152 (forward strand) | View in location tab

Co-located

with COSMIC COSM3466979 (T/C) ; HGMD-PUBLIC CM020680

Most severe consequence
Clinical significance

Synonyms

LSDB 1785

This variation has 13 HGVS names - click the plus to show

13:g.102868152T>C
ENST00000602836.1:c.3849T>C
ENSP00000473384.1:p.Leu1284Pro
ENST00000355739.6:c.2573T>C
ENSP00000347978.4:p.Leu858Pro
ENST00000481099.1:n.693T>C
ENST00000610537.2:c.2573T>C
ENSP00000478667.1:p.Leu858Pro
ENST00000375954.1:c.272T>C
ENSP00000365121.1:p.Leu91Pro
LRG_464:g.27329T>C
LRG_464t1:c.2573T>C
LRG_464p1:p.Glu864Gln

Variation displays