Product Details

SNP ID

rs202056255

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:150691794 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCAGCATGAGCTCCCATCCTCTGA[C/G]GGTCCTGAGAAGGATAGTGGATTGG

Phenotype

MIM: 612430

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

RBM22 PubMed Links

Gene Details

Gene

RBM22

Gene Name

RNA binding motif protein 22

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018047.2	1342	Missense Mutation	CCT,CGT	P407R	NP_060517.1

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