Product Details

SNP ID

rs141510669

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:178135256 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACCTCCCGGGCTCAAGCAGTCCTC[C/T]GTCCCACCTCAGCCTTCTGAGGAGC

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

N4BP3 PubMed Links

Additional Information

For this assay, SNP(s) [rs10060446] are located under a probe and SNP(s) [rs72536798] are located under a primer 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

N4BP3

Gene Name

NEDD4 binding protein 3

There are no transcripts associated with this gene.

Gene

RMND5B

Gene Name

required for meiotic nuclear division 5 homolog B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001288794.1	318	UTR 5			NP_001275723.1
NM_001288795.1	318	Missense Mutation	CCG,CTG	P15L	NP_001275724.1
NM_022762.4	318	Intron			NP_073599.2
XM_005265969.3	318	Intron			XP_005266026.1
XM_005265971.4	318	Intron			XP_005266028.1
XM_005265972.3	318	Intron			XP_005266029.1
XM_017009727.1	318	Intron			XP_016865216.1
XM_017009728.1	318	Intron			XP_016865217.1

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