Product Details

SNP ID

rs10108981

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:17251654 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCAGACAGTTAGTTTCTTCATAAAA[C/T]TAGGCATGATGCAGGTAAATAACCT

Phenotype

MIM: 604913 MIM: 609927

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CNOT7 PubMed Links

Additional Information

For this assay, SNP(s) [rs79130853] 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

CNOT7

Gene Name

CCR4-NOT transcription complex subunit 7

There are no transcripts associated with this gene.

Gene

VPS37A

Gene Name

VPS37A, ESCRT-I subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145152.1		Intron			NP_001138624.1
NM_152415.2		Intron			NP_689628.2
XM_005273400.2		Intron			XP_005273457.1
XM_005273401.2		Intron			XP_005273458.1
XM_006716286.1		Intron			XP_006716349.1
XM_017013021.1		Intron			XP_016868510.1
XM_017013022.1		Intron			XP_016868511.1
XM_017013023.1		Intron			XP_016868512.1
XM_017013024.1		Intron			XP_016868513.1
XM_017013025.1		Intron			XP_016868514.1
XM_017013026.1		Intron			XP_016868515.1

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