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SNP ID: rs7840192
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:66667560 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTCCTAGGATGCCGTGCGGTGCGTC[C/T]AGCTGCACTTCCTCCTTAGGCGGAG
Phenotype: MIM: 611745
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: C8orf44 PubMed Links

Gene Details

Gene: C8orf44
Gene Name: chromosome 8 open reading frame 44

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019607.2	9	UTR 5			NP_062553.1

Gene: C8orf44-SGK3
Gene Name: C8orf44-SGK3 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001204173.1	9	UTR 5			NP_001191102.1

Gene: VCPIP1
Gene Name: valosin containing protein interacting protein 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025054.4	9	Intron			NP_079330.2

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