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 4:6291961 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM983476

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13631, 2010_April_001_088_WFS1_606201_0010

This variation has 8 HGVS names - click the plus to show

4:g.6291961C>T
ENST00000507765.1:n.861C>T
ENST00000503569.3:c.676C>T
ENSP00000423337.1:p.Gln226Ter
ENST00000506362.1:c.273C>T
ENSP00000424103.1:p.Gln92Ter
ENST00000226760.3:c.676C>T
ENSP00000226760.1:p.Gln226Ter

Variation displays