Product Details

SNP ID

rs6695196

Assay Type

Functionally tested

NCBI dbSNP Submissions

20

Location

Chr.1:84300227 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAGATCAGCACTGGTGAAAGATCC[A/G]CATGCCTGACCCATGCTCAAAAAAT

Phenotype

Polymorphism

A/G, 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

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