Product Details

SNP ID

rs56926776

Assay Type

Functionally tested

NCBI dbSNP Submissions

10

Location

Chr.1:67702965 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTGTCTATCATTAACATAAACCA[A/G]CTGTTGCAGACAGTTAAACTGTGGC

Phenotype

MIM: 615405

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

GNG12 PubMed Links

Gene Details

Gene

GNG12

Gene Name

G protein subunit gamma 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018841.5	2910	UTR 3			NP_061329.3
XM_017001809.1	2910	UTR 3			XP_016857298.1
XM_017001810.1	2910	UTR 3			XP_016857299.1
XM_017001811.1	2910	UTR 3			XP_016857300.1

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