Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)
Location

Chromosome 11:111957665 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM003169

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 21 HGVS names - click the plus to show

11:g.111957665G>A
ENST00000528182.1:c.34G>A
ENSP00000435475.1:p.Gly12Ser
ENST00000525987.1:n.39G>A
ENST00000526592.1:c.34G>A
ENSP00000432005.1:p.Gly12Ser
HG388_HG400_PATCH:g.111957664G>A
ENST00000532699.1:c.34G>A
ENSP00000456434.1:p.Gly12Ser
ENST00000375549.3:c.34G>A
ENSP00000364699.3:p.Gly12Ser
ENST00000525291.1:c.34G>A
ENSP00000436669.1:p.Gly12Ser
ENST00000528021.1:c.34G>A
ENSP00000432465.1:p.Gly12Ser
ENST00000531744.1:c.34G>A
ENSP00000456957.1:p.Gly12Ser
ENST00000530923.1:c.24G>A
ENSP00000432946.1:p.Gly9Ser
ENST00000528048.1:c.34G>A
ENSP00000436217.1:p.Gly12Ser

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

Variation displays