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 11:44114237 (forward strand) | View in location tab

Co-located

with COSMIC COSM926969 (G/A), COSM926970 (G/A) ; HGMD-PUBLIC CM970453

Most severe consequence
Clinical significance

Synonyms

LSDB 15578

This variation has 15 HGVS names - click the plus to show

11:g.44114237G>A
ENST00000533608.2:c.679G>A
ENSP00000431173.1:p.Asp227Asn
ENST00000358681.5:c.679G>A
ENSP00000351509.4:p.Asp227Asn
ENST00000529186.1:n.377G>A
ENST00000395673.4:c.778G>A
ENSP00000379032.3:p.Asp260Asn
ENST00000343631.3:c.679G>A
ENSP00000342656.3:p.Asp227Asn
LRG_494:g.23689G>A
LRG_494t2.1:c.679G>A
LRG_494p2.1:p.Asp227Asn
LRG_494t1.1:c.778G>A
LRG_494p1.1:p.Asp260Asn

Variation displays