Product Details

SNP ID

rs61734695

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:164197497 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCAATACTTCCAGGCCCCCTGAG[A/T]CTCTTAGTTCAAGCTTTCTCAACTT

Phenotype

MIM: 606877 MIM: 613331

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

ANP32C PubMed Links

Additional Information

For this assay, SNP(s) [rs2288675] 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

ANP32C

Gene Name

acidic nuclear phosphoprotein 32 family member C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012403.1		Intron			NP_036535.1

Gene

MARCH1

Gene Name

membrane associated ring-CH-type finger 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001166373.1		Intron			NP_001159845.1
NM_017923.3		Intron			NP_060393.1
XM_011532055.2		Intron			XP_011530357.1
XM_017008334.1		Intron			XP_016863823.1
XM_017008335.1		Intron			XP_016863824.1
XM_017008336.1		Intron			XP_016863825.1

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