Product Details

SNP ID: rs9753600
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:36894870 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACTCATCTCTATTTCTACCCAGCTT[G/T]CTTTCTTTCTTTCTTTTTTTGAGAC
Phenotype: MIM: 606754
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: SAMHD1 PubMed Links

Gene Details

Gene: SAMHD1
Gene Name: SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015474.3		Intron			NP_056289.2
XM_005260384.3		Intron			XP_005260441.1
XM_011528761.2		Intron			XP_011527063.1

Gene: TLDC2
Gene Name: TBC/LysM-associated domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001304783.1		Intron			NP_001291712.1
NM_080628.2		Intron			NP_542195.1
XM_017027672.1		Intron			XP_016883161.1
XM_017027673.1		Intron			XP_016883162.1
XM_017027674.1		Intron			XP_016883163.1

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