Product Details

SNP ID
rs201238723
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:21126034 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACTCTCCGCAGCCACCTGGCAAGC[C/G]TTGGCCAGCTTTGCAGCCTTCTGGT
Phenotype
MIM: 605491
Polymorphism
C/G, Transversion 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_001010896.2 308 Missense Mutation ACG,AGG T86R NP_001010896.2
NM_001177483.1 308 UTR 3 NP_001170954.1
Gene
NEBL
Gene Name
nebulette
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001173484.1 308 Intron NP_001166955.1
NM_006393.2 308 Intron NP_006384.1
NM_213569.2 308 Intron NP_998734.1
XM_005252342.4 308 Intron XP_005252399.1
XM_005252343.4 308 Intron XP_005252400.1
XM_005252344.4 308 Intron XP_005252401.1
XM_011519291.2 308 Intron XP_011517593.1
XM_017015467.1 308 Intron XP_016870956.1
XM_017015468.1 308 Intron XP_016870957.1
XM_017015469.1 308 Intron XP_016870958.1

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