Product Details

SNP ID

rs17807992

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:92133833 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTACCTTATACCACATTTTTTGTA[A/G]CTATGGAGAGCACAGGTAGTAATAA

Phenotype

MIM: 606028

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CPSF2 PubMed Links

Gene Details

Gene

CPSF2

Gene Name

cleavage and polyadenylation specific factor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001322270.1		Intron			NP_001309199.1
NM_001322271.1		Intron			NP_001309200.1
NM_001322272.1		Intron			NP_001309201.1
NM_017437.2		Intron			NP_059133.1

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