Product Details

SNP ID

rs1596115

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:76230279 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCAGAGGGGATTATGGCCACCTCT[C/G]TCACTAAGAAAGTGGGGGAAAGCCA

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM47E PubMed Links

Gene Details

Gene

FAM47E

Gene Name

family with sequence similarity 47 member E

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136570.2		Intron			NP_001130042.1
NM_001242936.1		Intron			NP_001229865.1

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