Product Details

SNP ID

rs34677348

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:39352645 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGTTGGCCTGCTTTGTTCAAAGC[C/G]TGGCCTTGTAAGCATCATGTTTGAG

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

SAMD4B PubMed Links

Additional Information

For this assay, SNP(s) [rs75372153] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

SAMD4B

Gene Name

sterile alpha motif domain containing 4B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303614.1		Intron			NP_001290543.1
NM_018028.3		Intron			NP_060498.2
XM_011527057.2		Intron			XP_011525359.1
XM_011527060.2		Intron			XP_011525362.1
XM_011527061.2		Intron			XP_011525363.1
XM_011527062.2		Intron			XP_011525364.1
XM_011527063.2		Intron			XP_011525365.1
XM_011527064.2		Intron			XP_011525366.1
XM_017026918.1		Intron			XP_016882407.1
XM_017026919.1		Intron			XP_016882408.1
XM_017026920.1		Intron			XP_016882409.1
XM_017026921.1		Intron			XP_016882410.1
XM_017026922.1		Intron			XP_016882411.1
XM_017026923.1		Intron			XP_016882412.1

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