Original source

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

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

Chromosome 11:44135787 (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 10 HGVS names - click the plus to show

11:g.44135787G>A
ENST00000533608.1:c.679G>A
ENSP00000431173.1:p.Asp227Asn
ENST00000358681.4:c.679G>A
ENSP00000351509.4:p.Asp227Asn
ENST00000529186.1:n.377G>A
ENST00000395673.3:c.778G>A
ENSP00000379032.3:p.Asp260Asn
ENST00000343631.3:c.679G>A
ENSP00000342656.3:p.Asp227Asn

Variation displays