Product Details

SNP ID
rs9916499
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:21534776 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGTGACATCAGCCACTCCCCCCTAC[G/C]AACACCCATGCTTCAGGCCAGTCTG
Phenotype
Polymorphism
G/C, Transversion substitution
Allele Nomenclature
Literature Links
C17orf51 PubMed Links

Gene Details

Gene
C17orf51
Gene Name
chromosome 17 open reading frame 51
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001113434.4 1446 UTR 3 NP_001106905.1
XM_005256621.3 1446 Intron XP_005256678.1
XM_006721514.2 1446 Intron XP_006721577.1
XM_011523822.2 1446 Intron XP_011522124.1

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