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 4:6302281 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013445

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13636, 2010_April_001_091_WFS1_606201_0015

This variation has 6 HGVS names - click the plus to show

4:g.6302281T>C
ENST00000507765.1:n.2671T>C
ENST00000503569.2:c.2486T>C
ENSP00000423337.1:p.Leu829Pro
ENST00000226760.2:c.2486T>C
ENSP00000226760.1:p.Leu829Pro

Variation displays