Product Details

SNP ID

rs2765148

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:23986659 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATGTTTAGAGGTGTGGATTTCTCA[A/C]CTTTAATTTATCTTTTTGGTTTGCT

Phenotype

MIM: 613324

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

SPATA13 PubMed Links

Additional Information

For this assay, SNP(s) [rs77971723] 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

SPATA13

Gene Name

spermatogenesis associated 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001166271.2		Intron			NP_001159743.1
NM_001286792.1		Intron			NP_001273721.1
NM_001286793.1		Intron			NP_001273722.1
NM_001286794.1		Intron			NP_001273723.1
NM_001286795.1		Intron			NP_001273724.1
NM_153023.3		Intron			NP_694568.1

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