Product Details

SNP ID

rs8011690

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:67825190 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTGGCACAAGTGTAGCGCTCATAC[A/G]CACCTGGATTGGATGCTGGTGCTAT

Phenotype

MIM: 602948 MIM: 612012

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RAD51B PubMed Links

Additional Information

For this assay, SNP(s) [rs79415557] 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

RAD51B

Gene Name

RAD51 paralog B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321809.1		Intron			NP_001308738.1
NM_001321810.1		Intron			NP_001308739.1
NM_001321812.1		Intron			NP_001308741.1
NM_001321814.1		Intron			NP_001308743.1
NM_001321815.1		Intron			NP_001308744.1
NM_001321817.1		Intron			NP_001308746.1
NM_001321818.1		Intron			NP_001308747.1
NM_001321819.1		Intron			NP_001308748.1
NM_001321821.1		Intron			NP_001308750.1
NM_002877.5		Intron			NP_002868.1
NM_133509.3		Intron			NP_598193.2
NM_133510.3		Intron			NP_598194.1
XM_011537050.2		Intron			XP_011535352.1
XM_011537051.2		Intron			XP_011535353.1
XM_017021545.1		Intron			XP_016877034.1
XM_017021546.1		Intron			XP_016877035.1
XM_017021547.1		Intron			XP_016877036.1
XM_017021548.1		Intron			XP_016877037.1

Gene

ZFYVE26

Gene Name

zinc finger FYVE-type containing 26

There are no transcripts associated with this gene.

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