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SNP ID

rs145508824

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:187368461 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAAAAATGGTTGTAGATTTCTGGA[C/G]TTGGGAGCAGACATTTCAAGAACTA

Phenotype

MIM: 609350

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

RTP4 PubMed Links

Gene Details

Gene

RTP4

Gene Name

receptor transporter protein 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022147.2	82	Missense Mutation	ACT,AGT	T7S	NP_071430.2

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