Product Details

SNP ID

rs190327842

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:42743528 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTCTCTCTTCTTCTTCAAAGAAC[C/T]TTTGAGCTTCTTCCACAGGCTGTCT

Phenotype

MIM: 609592

Polymorphism

C/T, Transition 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	856	UTR 3			NP_001259006.1
NM_002930.3	856	Missense Mutation			NP_002921.1

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