Product Details

SNP ID
rs118072813
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:23765457 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAGTTGCATCAGCAAGAGGGGCAA[A/G]GTCAGACAGGATTTGAGGCCGCCAG
Phenotype
MIM: 615903 MIM: 185261
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C22orf15 PubMed Links

Gene Details

Gene
C22orf15
Gene Name
chromosome 22 open reading frame 15
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_182520.2 1406 Intron NP_872326.2
XM_011529907.2 1406 Silent Mutation AAA,AAG K242K XP_011528209.1
XM_011529908.2 1406 Silent Mutation AAA,AAG K177K XP_011528210.2
XM_011529912.2 1406 Silent Mutation AAA,AAG K189K XP_011528214.1
XM_017028602.1 1406 Silent Mutation AAA,AAG K270K XP_016884091.1
XM_017028603.1 1406 Silent Mutation AAA,AAG K263K XP_016884092.1
XM_017028604.1 1406 Silent Mutation AAA,AAG K250K XP_016884093.1
XM_017028605.1 1406 Silent Mutation AAA,AAG K247K XP_016884094.1
XM_017028606.1 1406 Silent Mutation AAA,AAG K270K XP_016884095.1
XM_017028607.1 1406 UTR 3 XP_016884096.1
XM_017028608.1 1406 Intron XP_016884097.1
XM_017028609.1 1406 Silent Mutation AAA,AAG K207K XP_016884098.1
XM_017028610.1 1406 Silent Mutation AAA,AAG K200K XP_016884099.1
XM_017028611.1 1406 Intron XP_016884100.1
XM_017028612.1 1406 Silent Mutation AAA,AAG K172K XP_016884101.1
XM_017028613.1 1406 Intron XP_016884102.1
XM_017028614.1 1406 Intron XP_016884103.1
XM_017028615.1 1406 Intron XP_016884104.1
XM_017028616.1 1406 Intron XP_016884105.1
XM_017028617.1 1406 Intron XP_016884106.1
XM_017028618.1 1406 Intron XP_016884107.1
Gene
CHCHD10
Gene Name
coiled-coil-helix-coiled-coil-helix domain containing 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001301339.1 1406 Intron NP_001288268.1
NM_213720.2 1406 Intron NP_998885.1
Gene
MMP11
Gene Name
matrix metallopeptidase 11
There are no transcripts associated with this gene.

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