Product Details

SNP ID

rs7905015

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:75103332 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTAGAAGACTCAGGCTGAGGGAAGC[A/G]GCACAGGCCCACACACAGACACAGG

Phenotype

MIM: 613191 MIM: 611575

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DUSP13 PubMed Links

Additional Information

For this assay, SNP(s) [rs145950091] 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

DUSP13

Gene Name

dual specificity phosphatase 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001007271.1		Intron			NP_001007272.1
NM_001007272.1		Intron			NP_001007273.1
NM_001007273.1		Intron			NP_001007274.1
NM_001320842.1		Intron			NP_001307771.1
NM_001320843.1		Intron			NP_001307772.1
NM_016364.3		Intron			NP_057448.3
XM_005269883.3		Intron			XP_005269940.1
XM_005269884.4		Intron			XP_005269941.3
XM_005269887.1		Intron			XP_005269944.1
XM_005269890.1		Intron			XP_005269947.1
XM_011539853.1		Intron			XP_011538155.1
XM_011539854.2		Intron			XP_011538156.1
XM_011539855.1		Intron			XP_011538157.1
XM_011539856.2		Intron			XP_011538158.1
XM_017016313.1		Intron			XP_016871802.1
XM_017016314.1		Intron			XP_016871803.1

Gene

SAMD8

Gene Name

sterile alpha motif domain containing 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001174156.1		Intron			NP_001167627.1
NM_144660.2		Intron			NP_653261.1
XM_005269541.4		Intron			XP_005269598.1
XM_011539311.1		Intron			XP_011537613.1
XM_011539312.2		Intron			XP_011537614.1
XM_017015738.1		Intron			XP_016871227.1
XM_017015739.1		Intron			XP_016871228.1

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