Product Details

SNP ID
rs112388598
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:29702241 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGGTAAACATGATTCCAGCATGGG[C/T]TGCTCCAAGGCCCTGAGACCCCAGG
Phenotype
MIM: 614297
Polymorphism
C/T, Transition 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 1273 UTR 3 NP_001026896.2
NM_001256046.1 1273 UTR 3 NP_001242975.1
NM_001256047.1 1273 UTR 3 NP_001242976.1
NM_001282929.1 1273 UTR 3 NP_001269858.1
NM_001282930.1 1273 UTR 3 NP_001269859.1
NM_001282931.1 1273 UTR 3 NP_001269860.1
NM_031448.4 1273 UTR 3 NP_113636.2

View Full Product Details