Product Details

SNP ID

rs475820

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:42745306 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAAGAAAAAAAACCTTCATTATTTT[A/C]AGCTGTTGACATTTTGCAATTGTTT

Phenotype

MIM: 609592

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

RIT2 PubMed Links

Gene Details

Gene

RIT2

Gene Name

Ras like without CAAX 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001272077.1		Intron			NP_001259006.1
NM_002930.3		Intron			NP_002921.1

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