Product Details

SNP ID
rs142863911
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:29701187 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTTTAGAAAAACATTTATTGTAA[G/T]CGATCACATTCAAGTCGTAGTTCTG
Phenotype
MIM: 614297
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
C19orf12 PubMed Links

Gene Details

Gene
C19orf12
Gene Name
chromosome 19 open reading frame 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001031726.3 2327 UTR 3 NP_001026896.2
NM_001256046.1 2327 UTR 3 NP_001242975.1
NM_001256047.1 2327 UTR 3 NP_001242976.1
NM_001282929.1 2327 UTR 3 NP_001269858.1
NM_001282930.1 2327 UTR 3 NP_001269859.1
NM_001282931.1 2327 UTR 3 NP_001269860.1
NM_031448.4 2327 UTR 3 NP_113636.2

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