Product Details

SNP ID

rs11738949

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:159157606 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAAATTCCCATAAAAAATTACATT[C/T]CCCCCTCCCCAGTTCTACCTGTAGC

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RNF145 PubMed Links

Additional Information

For this assay, SNP(s) [rs140766998] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

RNF145

Gene Name

ring finger protein 145

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199380.1	3269	UTR 3			NP_001186309.1
NM_001199381.1	3269	UTR 3			NP_001186310.1
NM_001199382.1	3269	UTR 3			NP_001186311.1
NM_001199383.1	3269	UTR 3			NP_001186312.1
NM_144726.2	3269	UTR 3			NP_653327.1
XM_017009138.1	3269	UTR 3			XP_016864627.1

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