Product Details

SNP ID
rs78094750
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:29700050 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCACTCAGCAAGGCCTGCTCCATC[A/G]GACACAAAACTGATCAGGAGTTGGA
Phenotype
MIM: 614297
Polymorphism
A/G, 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 3464 UTR 3 NP_001026896.2
NM_001256046.1 3464 UTR 3 NP_001242975.1
NM_001256047.1 3464 UTR 3 NP_001242976.1
NM_001282929.1 3464 UTR 3 NP_001269858.1
NM_001282930.1 3464 UTR 3 NP_001269859.1
NM_001282931.1 3464 UTR 3 NP_001269860.1
NM_031448.4 3464 UTR 3 NP_113636.2

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