Product Details

SNP ID
rs1051890
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:114400097 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTTGGCGGCTCCGGCCCCGGCCAT[C/T]TGGTTCCCTTGGGCTCCGGCCGCCA
Phenotype
MIM: 612413
Polymorphism
C/T, 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_001271562.1 454 Missense Mutation AAT,GAT N79D NP_001258491.1
NM_019021.3 454 Missense Mutation AAT,GAT N79D 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_001286045.1 454 Intron NP_001272974.1
NM_001286046.1 454 Intron NP_001272975.1
NM_001286047.1 454 Intron NP_001272976.1
NM_001286048.1 454 Intron NP_001272977.1
NM_016090.3 454 Intron NP_057174.1

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