Product Details

SNP ID
rs11591355
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:21126077 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTCTGGTCTCCCCAACCAGCTTCC[C/T]GGGAGGCCTCAGGCCCTTCTCGGCT
Phenotype
MIM: 605491
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C10orf113 PubMed Links

Gene Details

Gene
C10orf113
Gene Name
chromosome 10 open reading frame 113
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001010896.2 265 Missense Mutation AGG,GGG R72G NP_001010896.2
NM_001177483.1 265 UTR 3 NP_001170954.1
Gene
NEBL
Gene Name
nebulette
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001173484.1 265 Intron NP_001166955.1
NM_006393.2 265 Intron NP_006384.1
NM_213569.2 265 Intron NP_998734.1
XM_005252342.4 265 Intron XP_005252399.1
XM_005252343.4 265 Intron XP_005252400.1
XM_005252344.4 265 Intron XP_005252401.1
XM_011519291.2 265 Intron XP_011517593.1
XM_017015467.1 265 Intron XP_016870956.1
XM_017015468.1 265 Intron XP_016870957.1
XM_017015469.1 265 Intron XP_016870958.1

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