Product Details

SNP ID

rs9694

Assay Type

Functionally tested

NCBI dbSNP Submissions

66

Location

Chr.1:38839056 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTCTTCCGAGTTAGCAAGCAAATGC[A/G]TTTAAAAGGTCTTAGTTGTGCAATG

Phenotype

MIM: 608267

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RRAGC PubMed Links

Gene Details

Gene

RRAGC

Gene Name

Ras related GTP binding C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271851.1	1772	UTR 3			NP_001258780.1
NM_022157.3	1772	UTR 3			NP_071440.1

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