Product Details

SNP ID

rs5960479

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:55722705 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTCGTTGAAAGGTAAATTACGGTG[A/G]TGGGAAGGAAAGAAGTTAACTTGAT

Phenotype

MIM: 300725

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RRAGB PubMed Links

Gene Details

Gene

RRAGB

Gene Name

Ras related GTP binding B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006064.4		Intron			NP_006055.3
NM_016656.3		Intron			NP_057740.2
XM_005261973.4		Intron			XP_005262030.1
XM_017029217.1		Intron			XP_016884706.1
XM_017029218.1		Intron			XP_016884707.1

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