Product Details

SNP ID
rs2298374
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:23763985 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCACAGTCTTAGCCCATAGGCCCA[A/G]TCGCAGCTCTGGGAAAGGGAGAGAT
Phenotype
MIM: 615903 MIM: 185261 MIM: 605017
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_182520.2 980 Intron NP_872326.2
XM_011529907.2 980 Missense Mutation AAT,AGT N38S XP_011528209.1
XM_011529908.2 980 Intron XP_011528210.2
XM_011529912.2 980 Missense Mutation AAT,AGT N38S XP_011528214.1
XM_017028602.1 980 Missense Mutation AAT,AGT N38S XP_016884091.1
XM_017028603.1 980 Missense Mutation AAT,AGT N38S XP_016884092.1
XM_017028604.1 980 Missense Mutation AAT,AGT N38S XP_016884093.1
XM_017028605.1 980 Missense Mutation AAT,AGT N38S XP_016884094.1
XM_017028606.1 980 Missense Mutation AAT,AGT N38S XP_016884095.1
XM_017028607.1 980 Missense Mutation AAT,AGT N38S XP_016884096.1
XM_017028608.1 980 Missense Mutation AAT,AGT N38S XP_016884097.1
XM_017028609.1 980 Intron XP_016884098.1
XM_017028610.1 980 Intron XP_016884099.1
XM_017028611.1 980 Missense Mutation AAT,AGT N38S XP_016884100.1
XM_017028612.1 980 Intron XP_016884101.1
XM_017028613.1 980 Missense Mutation AAT,AGT N38S XP_016884102.1
XM_017028614.1 980 Missense Mutation AAT,AGT N38S XP_016884103.1
XM_017028615.1 980 Intron XP_016884104.1
XM_017028616.1 980 Intron XP_016884105.1
XM_017028617.1 980 Intron XP_016884106.1
XM_017028618.1 980 Intron 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.

Gene
VPREB3
Gene Name
pre-B lymphocyte 3
There are no transcripts associated with this gene.

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