Product Details

SNP ID
rs9389382
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:136342640 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCTATCCTATATGCTTAATCAACAG[C/G]AGGCTAGGAAAATGTCACTGAGTTA
Phenotype
MIM: 604108
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
MAP7 PubMed Links

Gene Details

Gene
MAP7
Gene Name
microtubule associated protein 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001198608.1 3889 UTR 3 NP_001185537.1
NM_001198609.1 3889 UTR 3 NP_001185538.1
NM_001198611.1 3889 UTR 3 NP_001185540.1
NM_001198614.1 3889 UTR 3 NP_001185543.1
NM_001198615.1 3889 UTR 3 NP_001185544.1
NM_001198616.1 3889 UTR 3 NP_001185545.1
NM_001198617.1 3889 UTR 3 NP_001185546.1
NM_001198618.1 3889 UTR 3 NP_001185547.1
NM_001198619.1 3889 UTR 3 NP_001185548.1
NM_003980.4 3889 UTR 3 NP_003971.1
XM_006715598.2 3889 Intron XP_006715661.1
XM_006715599.2 3889 Intron XP_006715662.1
XM_006715600.2 3889 Intron XP_006715663.1
XM_006715601.3 3889 Intron XP_006715664.1
XM_011536243.2 3889 Intron XP_011534545.1
XM_011536244.2 3889 Intron XP_011534546.1
XM_011536245.1 3889 Intron XP_011534547.1
XM_011536246.2 3889 Intron XP_011534548.1
XM_017011471.1 3889 Intron XP_016866960.1

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