Product Details

SNP ID
rs145421387
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:75587119 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGTTGGGATCATGACTCGGGGTAG[A/T]GGTGAGACAGTAGGTAGCTGAGGGT
Phenotype
MIM: 601783
Polymorphism
A/T, Transversion 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 5034 Silent Mutation CCA,CCT P794P NP_149052.1
NM_207577.1 5034 Intron NP_997460.1
XM_006718556.3 5034 Intron XP_006718619.1
XM_011545039.2 5034 Intron XP_011543341.1
XM_017017755.1 5034 Silent Mutation CCA,CCT P810P XP_016873244.1
XM_017017756.1 5034 Silent Mutation CCA,CCT P509P XP_016873245.1
XM_017017757.1 5034 Silent Mutation CCA,CCT P493P XP_016873246.1
XM_017017758.1 5034 Silent Mutation CCA,CCT P481P XP_016873247.1

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