Product Details

SNP ID
rs74868577
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:29699141 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCATTGATACAGGTGTTCAAAGGG[A/G]CATATAGGATAAGAAGGCAAGTACG
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 4373 UTR 3 NP_001026896.2
NM_001256046.1 4373 UTR 3 NP_001242975.1
NM_001256047.1 4373 UTR 3 NP_001242976.1
NM_001282929.1 4373 UTR 3 NP_001269858.1
NM_001282930.1 4373 UTR 3 NP_001269859.1
NM_001282931.1 4373 UTR 3 NP_001269860.1
NM_031448.4 4373 UTR 3 NP_113636.2

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