Product Details

SNP ID
rs200041937
Assay Type
Functionally Tested
NCBI dbSNP Submissions
4
Location
Chr.1:37692759 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTACGGAGGCGGAAGCTCGCCTC[C/T]TTTCTGAAAGACTTCGACCGTGAAG
Phenotype
MIM: 614799 MIM: 609977
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
C1orf109 PubMed Links

Gene Details

Gene
C1orf109
Gene Name
chromosome 1 open reading frame 109
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001303030.1 262 Intron NP_001289959.1
NM_001303031.1 262 Intron NP_001289960.1
NM_017850.2 262 Intron NP_060320.1
XM_005270975.4 262 Intron XP_005271032.1
XM_005270979.1 262 Intron XP_005271036.1
XM_005270980.1 262 Intron XP_005271037.1
XM_005270981.4 262 Intron XP_005271038.1
XM_005270982.1 262 Intron XP_005271039.1
XM_011541637.1 262 Intron XP_011539939.1
XM_011541638.1 262 Intron XP_011539940.1
XM_011541639.1 262 Intron XP_011539941.1
XM_011541640.1 262 Intron XP_011539942.1
XM_011541641.1 262 Intron XP_011539943.1
XM_011541642.1 262 Intron XP_011539944.1
XM_011541643.1 262 Intron XP_011539945.1
XM_011541646.2 262 Intron XP_011539948.1
XM_017001544.1 262 Intron XP_016857033.1
XM_017001545.1 262 Intron XP_016857034.1
XM_017001546.1 262 Intron XP_016857035.1
XM_017001547.1 262 Intron XP_016857036.1
XM_017001548.1 262 Intron XP_016857037.1
XM_017001549.1 262 Intron XP_016857038.1
XM_017001550.1 262 Intron XP_016857039.1
XM_017001551.1 262 Intron XP_016857040.1
XM_017001552.1 262 Intron XP_016857041.1
XM_017001553.1 262 Intron XP_016857042.1
XM_017001554.1 262 Intron XP_016857043.1
XM_017001555.1 262 Intron XP_016857044.1
XM_017001556.1 262 Intron XP_016857045.1
Gene
CDCA8
Gene Name
cell division cycle associated 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256875.1 262 Silent Mutation TCC,TCT S23S NP_001243804.1
NM_018101.3 262 Silent Mutation TCC,TCT S23S NP_060571.1

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