Product Details

SNP ID
rs17032851
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:155344087 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCTTGGGAATGATTATAACTAACA[C/T]GTAATTTCCCCTACTTTGTGAAATT
Phenotype
MIM: 610070
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MAP9 PubMed Links

Gene Details

Gene
MAP9
Gene Name
microtubule associated protein 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039580.1 5921 UTR 3 NP_001034669.1
XM_006714306.3 5921 Intron XP_006714369.1
XM_011532253.1 5921 UTR 3 XP_011530555.1
XM_011532254.2 5921 UTR 3 XP_011530556.1
XM_011532255.2 5921 UTR 3 XP_011530557.1
XM_017008616.1 5921 Intron XP_016864105.1
XM_017008617.1 5921 UTR 3 XP_016864106.1
XM_017008618.1 5921 Intron XP_016864107.1

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