Product Details

SNP ID
rs147198204
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:93926113 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGGTGTCTAAATGTTCTGAAGAAA[C/T]AAAGAACTATATTGAAGAACGTTCT
Phenotype
MIM: 604390
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
GNG11 PubMed Links

Gene Details

Gene
GNG11
Gene Name
G protein subunit gamma 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004126.3 553 Missense Mutation ACA,ATA T40I NP_004117.1

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