Product Details

SNP ID
rs139688522
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:37215212 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAATACTCACTCAGCAGACATCTA[C/T]TGTGTATCTACAGGTGCTGGGGGCT
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TMEM217 PubMed Links

Gene Details

Gene
TMEM217
Gene Name
transmembrane protein 217
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001162900.1 743 Intron NP_001156372.1
NM_001286401.1 743 Intron NP_001273330.1
NM_145316.3 743 Missense Mutation ATA,GTA I226V NP_660359.2
XM_011514362.1 743 Silent Mutation CAA,CAG Q234Q XP_011512664.1
XM_011514363.2 743 Silent Mutation CAA,CAG Q234Q XP_011512665.1
XM_011514364.2 743 Silent Mutation CAA,CAG Q234Q XP_011512666.1
XM_011514365.2 743 Silent Mutation CAA,CAG Q234Q XP_011512667.1
XM_011514366.2 743 Missense Mutation ATA,GTA I226V XP_011512668.1
XM_011514367.2 743 Intron XP_011512669.1
XM_011514369.2 743 Intron XP_011512671.1
XM_011514370.2 743 Intron XP_011512672.1

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