Product Details

SNP ID: rs2169479
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.15:34342999 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTACATTTCTCGCCATGCCTATTTA[C/T]ACCCTGTTTTCTCTCCTCACCTTCA
Phenotype: MIM: 606471 MIM: 608963 MIM: 604878
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: NOP10 PubMed Links

Gene Details

Gene: NOP10
Gene Name: NOP10 ribonucleoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018648.3		Intron			NP_061118.1

Gene: NUTM1
Gene Name: NUT midline carcinoma family member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001284292.1		Intron			NP_001271221.1
NM_001284293.1		Intron			NP_001271222.1
NM_175741.2		Intron			NP_786883.1

Gene: SLC12A6
Gene Name: solute carrier family 12 member 6

There are no transcripts associated with this gene.

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