Product Details

SNP ID

rs4907056

Assay Type

Functionally tested

NCBI dbSNP Submissions

17

Location

Chr.1:84308231 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCATTACTCCATCTTGACTGGAAG[C/T]AGAAGTTCCATTTAATTTATATAGC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SAMD13 PubMed Links

Gene Details

Gene

SAMD13

Gene Name

sterile alpha motif domain containing 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010971.2		Intron			NP_001010971.1
NM_001134663.1		Intron			NP_001128135.1
NM_001134664.1		Intron			NP_001128136.1
XM_017000377.1		Intron			XP_016855866.1

View Full Product Details