Original source

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

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

Chromosome 13:103520502 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020680

Most severe consequence
Clinical significance

Synonyms

LSDB 1785

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

13:g.103520502T>C
ENST00000602836.1:c.3849T>C
ENSP00000473384.1:p.Leu1284Pro
ENST00000355739.4:c.2573T>C
ENSP00000347978.4:p.Leu858Pro
ENST00000481099.1:n.693T>C
ENST00000375954.1:c.272T>C
ENSP00000365121.1:p.Leu91Pro
LRG_464:g.27329T>C
LRG_464t1.1:c.2573T>C
LRG_464p1.1:p.Leu858Pro

Variation displays