Product Details

SNP ID
rs138750180
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:75587083 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCAAGGGGAGCTCTCAATGTATTC[C/T]GTATGGGGGGCAGTTGGGATCATGA
Phenotype
MIM: 601783
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MAP6 PubMed Links

Gene Details

Gene
MAP6
Gene Name
microtubule associated protein 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_033063.1 5070 Silent Mutation ACA,ACG T806T NP_149052.1
NM_207577.1 5070 Intron NP_997460.1
XM_006718556.3 5070 Intron XP_006718619.1
XM_011545039.2 5070 Intron XP_011543341.1
XM_017017755.1 5070 Silent Mutation ACA,ACG T822T XP_016873244.1
XM_017017756.1 5070 Silent Mutation ACA,ACG T521T XP_016873245.1
XM_017017757.1 5070 Silent Mutation ACA,ACG T505T XP_016873246.1
XM_017017758.1 5070 Silent Mutation ACA,ACG T493T XP_016873247.1

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