Product Details

SNP ID
rs41279096
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:121002460 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGCAGCTTGTAGCCAGCCGGGGC[A/G]AGTGGCACGTTTATTTAACTTTTAG
Phenotype
MIM: 142410
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C12orf43 PubMed Links

Gene Details

Gene
C12orf43
Gene Name
chromosome 12 open reading frame 43
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286191.1 2414 UTR 3 NP_001273120.1
NM_001286192.1 2414 UTR 3 NP_001273121.1
NM_001286195.1 2414 UTR 3 NP_001273124.1
NM_001286196.1 2414 UTR 3 NP_001273125.1
NM_001286197.1 2414 UTR 3 NP_001273126.1
NM_001286198.1 2414 UTR 3 NP_001273127.1
NM_022895.2 2414 UTR 3 NP_075046.1
XM_017019829.1 2414 Intron XP_016875318.1
Gene
HNF1A
Gene Name
HNF1 homeobox A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000545.6 2414 UTR 3 NP_000536.5
NM_001306179.1 2414 UTR 3 NP_001293108.1
XM_005253931.3 2414 UTR 3 XP_005253988.1

View Full Product Details