Product Details

SNP ID

rs370616063

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:39636231 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGTGAAAATACTGCAAGAATTCG[A/G]TCTCCGAGAACTTATTTTAATTAGG

Phenotype

MIM: 601081

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ABCD2 PubMed Links

Additional Information

For this assay, SNP(s) [rs373965264] 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

ABCD2

Gene Name

ATP binding cassette subfamily D member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005164.3		Intron			NP_005155.1
XM_011538027.2		Intron			XP_011536329.1
XM_017018992.1		Intron			XP_016874481.1
XM_017018993.1		Intron			XP_016874482.1
XM_017018994.1		Intron			XP_016874483.1

Gene

C12orf40

Gene Name

chromosome 12 open reading frame 40

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001031748.3		Intron			NP_001026918.2
NM_001319247.1		Intron			NP_001306176.1
XM_005268806.3		Intron			XP_005268863.1
XM_011538231.2		Intron			XP_011536533.1

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