Product Details

SNP ID
rs140994962
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:75587561 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTGGCCATGGCACTTTCATCCTTC[A/G]GATGCTCTGGGACCATGGGATCTTG
Phenotype
MIM: 601783
Polymorphism
A/G, 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 4592 Missense Mutation CCG,CTG P647L NP_149052.1
NM_207577.1 4592 Intron NP_997460.1
XM_006718556.3 4592 Intron XP_006718619.1
XM_011545039.2 4592 Intron XP_011543341.1
XM_017017755.1 4592 Missense Mutation CCG,CTG P663L XP_016873244.1
XM_017017756.1 4592 Missense Mutation CCG,CTG P362L XP_016873245.1
XM_017017757.1 4592 Missense Mutation CCG,CTG P346L XP_016873246.1
XM_017017758.1 4592 Missense Mutation CCG,CTG P334L XP_016873247.1

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