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SNP ID: rs12664567
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:13624348 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AGTCTCCCTATCTAAACTACTCTTT[A/C]ATCTACTTTTTGTGGCACTGCCCTC
Phenotype: MIM: 611533 MIM: 603854 MIM: 604483
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: NOL7 PubMed Links

Gene Details

Gene: NOL7
Gene Name: nucleolar protein 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317724.1		Intron			NP_001304653.1
NM_016167.4		Intron			NP_057251.2

Gene: RANBP9
Gene Name: RAN binding protein 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005493.2		Intron			NP_005484.2
XM_006714945.2		Intron			XP_006715008.1
XM_011514205.2		Intron			XP_011512507.1
XM_017010149.1		Intron			XP_016865638.1

Gene: SIRT5
Gene Name: sirtuin 5

There are no transcripts associated with this gene.

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