Product Details

SNP ID

rs689116

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:218569165 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGCCGGCCCCTATTTCCTTGCCGGA[A/C]GCCTCTCGCGGCCTTCAGCGCGACC

Phenotype

MIM: 612054

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

CNOT9 PubMed Links

Gene Details

Gene

CNOT9

Gene Name

CCR4-NOT transcription complex subunit 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271634.1		Intron			NP_001258563.1
NM_001271635.1		Intron			NP_001258564.1
NM_005444.2		Intron			NP_005435.1
XM_011512138.2		Intron			XP_011510440.1
XM_017005248.1		Intron			XP_016860737.1
XM_017005249.1		Intron			XP_016860738.1

Gene

USP37

Gene Name

ubiquitin specific peptidase 37

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020935.2		Intron			NP_065986.2
XM_005246720.2		Intron			XP_005246777.1
XM_005246721.3		Intron			XP_005246778.1
XM_005246722.3		Intron			XP_005246779.1
XM_005246724.1		Intron			XP_005246781.1
XM_011511538.2		Intron			XP_011509840.1
XM_011511541.2		Intron			XP_011509843.1
XM_017004577.1		Intron			XP_016860066.1

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