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 7:94049588 (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 10 HGVS names - click the plus to show

7:g.94049588G>A
ENST00000297268.6:c.2123G>A
ENSP00000297268.6:p.Arg708Gln
ENST00000473573.1:n.460G>A
ENST00000461525.1:n.212G>A
ENST00000497316.1:n.520G>A
ENST00000467931.1:n.143G>A
LRG_2:g.30716G>A
LRG_2t1.1:c.2123G>A
LRG_2p1.1:p.Arg708Gln

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays