Product Details

SNP ID

rs6986660

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:41496002 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGGAACCAGAAGTATTTCAGTTTT[G/T]GGGGTTTTTTTAGATTTTGAAATAT

Phenotype

MIM: 609453

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

GOLGA7 PubMed Links

Gene Details

Gene

GOLGA7

Gene Name

golgin A7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002296.1		Intron			NP_001002296.1
NM_001174124.1		Intron			NP_001167595.1
NM_016099.2		Intron			NP_057183.2

View Full Product Details