Product Details

SNP ID

rs16866179

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:38843817 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTAGTTAAATAATATAAAATAAAT[G/T]TTCTGAAAACTAATCTGCCTTTGGG

Phenotype

MIM: 608267

Polymorphism

G/T, Transversion 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		Intron			NP_001258780.1
NM_022157.3		Intron			NP_071440.1

View Full Product Details