Product Details

SNP ID

rs4499339

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:40299414 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTAACCAGACTAATTATTAGTGAC[C/G]TAAATTAATAGTTACCTGAGATCCT

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C19orf47 PubMed Links

Gene Details

Gene

C19orf47

Gene Name

chromosome 19 open reading frame 47

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256440.1		Intron			NP_001243369.1
NM_001256441.1		Intron			NP_001243370.1

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