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ACAACATCTTGATCCTTGACTGGCC[C/G]TGAGACCACTAAACCTTGATTCTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601783 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MAP6 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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MAP6 - microtubule associated protein 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033063.1 | 4684 | Missense Mutation | CGG,GGG | R,G 678 | NP_149052.1 | |
NM_207577.1 | 4684 | Intron | NP_997460.1 | |||
XM_006718556.3 | 4684 | Intron | XP_006718619.1 | |||
XM_011545039.2 | 4684 | Intron | XP_011543341.1 | |||
XM_017017755.1 | 4684 | Missense Mutation | CGG,GGG | R,G 694 | XP_016873244.1 | |
XM_017017756.1 | 4684 | Missense Mutation | CGG,GGG | R,G 393 | XP_016873245.1 | |
XM_017017757.1 | 4684 | Missense Mutation | CGG,GGG | R,G 377 | XP_016873246.1 | |
XM_017017758.1 | 4684 | Missense Mutation | CGG,GGG | R,G 365 | XP_016873247.1 |