Product Details

SNP ID
rs10426842
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:40304790 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCCAGTCAAAGAACCTAGAAGGGTA[C/G]AGGGAAGCCATTTTTTGCTCCCCTA
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
C19orf47 PubMed Links

Gene Details

Gene
C19orf47
Gene Name
chromosome 19 open reading frame 47
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256440.1 Intron NP_001243369.1
NM_001256441.1 Intron NP_001243370.1
XM_005258520.2 Intron XP_005258577.1
XM_011526460.2 Intron XP_011524762.1
XM_017026291.1 Intron XP_016881780.1
XM_017026292.1 Intron XP_016881781.1
XM_017026293.1 Intron XP_016881782.1
XM_017026294.1 Intron XP_016881783.1
XM_017026295.1 Intron XP_016881784.1

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