Product Details

SNP ID
rs8112998
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:40318658 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTGGCAATGACCTGAAGGGGCGGCC[C/T]CTGGAATCTGAGGGCCAGCATTTGC
Phenotype
Polymorphism
C/T, Transition 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 3829 Intron NP_001243369.1
NM_001256441.1 3829 Intron NP_001243370.1
XM_005258520.2 3829 Intron XP_005258577.1
XM_011526460.2 3829 Intron XP_011524762.1
XM_017026291.1 3829 Intron XP_016881780.1
XM_017026292.1 3829 UTR 3 XP_016881781.1
XM_017026293.1 3829 UTR 3 XP_016881782.1
XM_017026294.1 3829 Intron XP_016881783.1
XM_017026295.1 3829 Intron XP_016881784.1

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