Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 4:6302385 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062036, CM043882

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_006005.2:c.2590G>A, 13641, 2010_April_001_095_WFS1_606201_0020

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

4:g.6302385G>A
ENST00000507765.1:n.2775G>A
ENST00000503569.3:c.2590G>A
ENSP00000423337.1:p.Glu864Lys
ENST00000226760.3:c.2590G>A
ENSP00000226760.1:p.Glu864Lys

Variation displays