Product Details

SNP ID
rs78697128
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:10572471 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAGGGCCCTGACAGACCAGCCTCC[G/T]ACAAAGTAGGAGACTGGTTTTTCAA
Phenotype
MIM: 616197
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
NOL10 PubMed Links

Gene Details

Gene
NOL10
Gene Name
nucleolar protein 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001261392.1 Intron NP_001248321.1
NM_001261394.1 Intron NP_001248323.1
NM_024894.3 Intron NP_079170.2
XM_011510398.2 Intron XP_011508700.1
XM_011510399.2 Intron XP_011508701.1
XM_011510400.2 Intron XP_011508702.1
XM_011510402.2 Intron XP_011508704.1
XM_017004990.1 Intron XP_016860479.1
XM_017004991.1 Intron XP_016860480.1

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