Product Details

SNP ID
rs12951898
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:54958241 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CGAGTACAACTGTGAAGAACAGTGC[C/T]AGGGGCAGACAAGTAAGATAAGAAC
Phenotype
MIM: 603648 MIM: 604701
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
COX11 PubMed Links

Gene Details

Gene
COX11
Gene Name
COX11, cytochrome c oxidase copper chaperone
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001162861.2 2206 Intron NP_001156333.1
NM_001162862.2 2206 Intron NP_001156334.1
NM_001321518.1 2206 Intron NP_001308447.1
NM_004375.4 2206 Intron NP_004366.1
XM_011524342.2 2206 UTR 3 XP_011522644.1
XM_017024192.1 2206 UTR 3 XP_016879681.1
XM_017024193.1 2206 Intron XP_016879682.1
XM_017024194.1 2206 UTR 3 XP_016879683.1
XM_017024195.1 2206 UTR 3 XP_016879684.1
XM_017024196.1 2206 Intron XP_016879685.1
Gene
TOM1L1
Gene Name
target of myb1 like 1 membrane trafficking protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321173.1 2206 Intron NP_001308102.1
NM_001321174.1 2206 Intron NP_001308103.1
NM_001321175.1 2206 Intron NP_001308104.1
NM_001321176.1 2206 Intron NP_001308105.1
NM_005486.2 2206 Intron NP_005477.2
XM_017024002.1 2206 Intron XP_016879491.1

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