Product Details

SNP ID
rs200130893
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:114400672 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGTTAGGGAGGGGGCGACGCTGAG[A/G]TGGGGGCGGCGGCGGCGGAAGCGGA
Phenotype
MIM: 612413
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C11orf71 PubMed Links

Gene Details

Gene
C11orf71
Gene Name
chromosome 11 open reading frame 71
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001271562.1 144 Intron NP_001258491.1
NM_019021.3 144 Intron NP_061894.2
Gene
RBM7
Gene Name
RNA binding motif protein 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286045.1 144 Missense Mutation ATG,GTG M1V NP_001272974.1
NM_001286046.1 144 UTR 5 NP_001272975.1
NM_001286047.1 144 UTR 5 NP_001272976.1
NM_001286048.1 144 UTR 5 NP_001272977.1
NM_016090.3 144 Missense Mutation ATG,GTG M1V NP_057174.1

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