Product Details

SNP ID
rs7291060
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:23764499 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CAAGGCCCTGTCCGGCCTCCCACCT[C/T]GGCTGGGGACCTAGCCCCAATCCAT
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_182520.2 659 Intron NP_872326.2
XM_011529907.2 659 Intron XP_011528209.1
XM_011529908.2 659 Intron XP_011528210.2
XM_011529912.2 659 Intron XP_011528214.1
XM_017028602.1 659 Intron XP_016884091.1
XM_017028603.1 659 Intron XP_016884092.1
XM_017028604.1 659 Intron XP_016884093.1
XM_017028605.1 659 Intron XP_016884094.1
XM_017028606.1 659 Intron XP_016884095.1
XM_017028607.1 659 Intron XP_016884096.1
XM_017028608.1 659 Intron XP_016884097.1
XM_017028609.1 659 Intron XP_016884098.1
XM_017028610.1 659 Intron XP_016884099.1
XM_017028611.1 659 Intron XP_016884100.1
XM_017028612.1 659 Intron XP_016884101.1
XM_017028613.1 659 Intron XP_016884102.1
XM_017028614.1 659 Intron XP_016884103.1
XM_017028615.1 659 Intron XP_016884104.1
XM_017028616.1 659 Intron XP_016884105.1
XM_017028617.1 659 Intron XP_016884106.1
XM_017028618.1 659 UTR 3 XP_016884107.1
Gene
CHCHD10
Gene Name
coiled-coil-helix-coiled-coil-helix domain containing 10
There are no transcripts associated with this gene.

Gene
MMP11
Gene Name
matrix metallopeptidase 11
There are no transcripts associated with this gene.

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