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 7:94420276 (forward strand) | View in location tab

Co-located

with COSMIC COSM388431 (G/T) ; HGMD-PUBLIC CM900074

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

7:g.94420276G>A
ENST00000473573.3:n.460G>A
ENST00000297268.8:c.2123G>A
ENSP00000297268.6:p.Arg708Gln
ENST00000620463.1:c.2117G>A
ENSP00000477719.1:p.Arg706Gln
ENST00000461525.3:n.212G>A
ENST00000497316.3:n.520G>A
ENST00000467931.1:n.143G>A
LRG_2:g.30716G>A
LRG_2t1:c.2123G>A
LRG_2p1:p.Arg708Gln

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays