Product Details

SNP ID

rs1156085

Assay Type

Functionally tested

NCBI dbSNP Submissions

32

Location

Chr.1:84298566 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AACCTCCCGGCGCGGCCATGCGGGG[A/G]GGTAAGTGATCTGCCTGTGCGCCCA

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	201	Silent Mutation	GGA,GGG	G3G	NP_001010971.1
NM_001134663.1	201	Intron			NP_001128135.1
NM_001134664.1	201	Intron			NP_001128136.1
XM_017000377.1	201	Intron			XP_016855866.1

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