Product Details

SNP ID
rs150794285
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:102047838 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGTCCATGCTGGGCAGAATCAAGG[C/T]GCAGGCGTTCGGCTTTGACCAGACC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C11orf70 PubMed Links

Gene Details

Gene
C11orf70
Gene Name
chromosome 11 open reading frame 70
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001195005.1 196 Missense Mutation GCG,GTG A45V NP_001181934.1
NM_032930.2 196 Missense Mutation GCG,GTG A45V NP_116319.2
XM_005271713.3 196 Missense Mutation GCG,GTG A45V XP_005271770.1
XM_017018454.1 196 Missense Mutation GCG,GTG A45V XP_016873943.1

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