Product Details

SNP ID
rs17374347
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:36837483 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGACTCAGGGTGGGAATCCCTGC[C/G]CTCAAATGCTTACACAGTTGCTTTG
Phenotype
MIM: 616642 MIM: 604209
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
C6orf89 PubMed Links

Gene Details

Gene
C6orf89
Gene Name
chromosome 6 open reading frame 89
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286635.1 Intron NP_001273564.1
NM_001286636.1 Intron NP_001273565.1
NM_001286637.1 Intron NP_001273566.1
NM_152734.3 Intron NP_689947.2
XM_011514377.2 Intron XP_011512679.1
XM_017010432.1 Intron XP_016865921.1
XM_017010433.1 Intron XP_016865922.1
XM_017010434.1 Intron XP_016865923.1
Gene
CPNE5
Gene Name
copine 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001314017.1 Intron NP_001300946.1
NM_001314018.1 Intron NP_001300947.1
NM_001314019.1 Intron NP_001300948.1
NM_001314020.1 Intron NP_001300949.1
NM_020939.1 Intron NP_065990.1
XM_005249247.2 Intron XP_005249304.1
XM_011514768.1 Intron XP_011513070.1
XM_011514769.1 Intron XP_011513071.1
XM_011514770.1 Intron XP_011513072.1
XM_011514771.2 Intron XP_011513073.1
XM_011514772.1 Intron XP_011513074.1
XM_011514773.2 Intron XP_011513075.1
XM_011514775.2 Intron XP_011513077.1
XM_017011139.1 Intron XP_016866628.1

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