Product Details

SNP ID
rs191584876
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:10572115 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTTGTGTCTTGACTTCAGGTGTC[C/T]GGCCGAACGACGGAGTCTTTTCCTT
Phenotype
MIM: 616197
Polymorphism
C/T, Transition 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 1674 Missense Mutation AGA,GGA R649G NP_001248321.1
NM_001261394.1 1674 Missense Mutation AGA,GGA R625G NP_001248323.1
NM_024894.3 1674 Missense Mutation AGA,GGA R675G NP_079170.2
XM_011510398.2 1674 Missense Mutation AGA,GGA R525G XP_011508700.1
XM_011510399.2 1674 Missense Mutation AGA,GGA R525G XP_011508701.1
XM_011510400.2 1674 Intron XP_011508702.1
XM_011510402.2 1674 Intron XP_011508704.1
XM_017004990.1 1674 Missense Mutation AGA,GGA R350G XP_016860479.1
XM_017004991.1 1674 Missense Mutation AGA,GGA R350G XP_016860480.1

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