Product Details

SNP ID
rs1054055
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:23765747 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCCCTGATTAAGGGGATGGATTGCA[C/T]ACTGTAGTGAGACATCCATCCTGAC
Phenotype
MIM: 615903 MIM: 185261
Polymorphism
C/T, 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 1444 UTR 3 NP_872326.2
XM_011529907.2 1444 UTR 3 XP_011528209.1
XM_011529908.2 1444 UTR 3 XP_011528210.2
XM_011529912.2 1444 UTR 3 XP_011528214.1
XM_017028602.1 1444 UTR 3 XP_016884091.1
XM_017028603.1 1444 UTR 3 XP_016884092.1
XM_017028604.1 1444 UTR 3 XP_016884093.1
XM_017028605.1 1444 UTR 3 XP_016884094.1
XM_017028606.1 1444 UTR 3 XP_016884095.1
XM_017028607.1 1444 UTR 3 XP_016884096.1
XM_017028608.1 1444 UTR 3 XP_016884097.1
XM_017028609.1 1444 UTR 3 XP_016884098.1
XM_017028610.1 1444 UTR 3 XP_016884099.1
XM_017028611.1 1444 Missense Mutation ACA,ATA T226I XP_016884100.1
XM_017028612.1 1444 UTR 3 XP_016884101.1
XM_017028613.1 1444 UTR 3 XP_016884102.1
XM_017028614.1 1444 UTR 3 XP_016884103.1
XM_017028615.1 1444 Missense Mutation ACA,ATA T156I XP_016884104.1
XM_017028616.1 1444 UTR 3 XP_016884105.1
XM_017028617.1 1444 UTR 3 XP_016884106.1
XM_017028618.1 1444 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 1444 Intron NP_001288268.1
NM_213720.2 1444 Intron NP_998885.1
Gene
MMP11
Gene Name
matrix metallopeptidase 11
There are no transcripts associated with this gene.

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