Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTGGCCATGGCACTTTCATCCTTC[A/G]GATGCTCTGGGACCATGGGATCTTG
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 4592 | Missense Mutation | CCG,CTG | P,L 647 | 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 | P,L 663 | XP_016873244.1 | |
XM_017017756.1 | 4592 | Missense Mutation | CCG,CTG | P,L 362 | XP_016873245.1 | |
XM_017017757.1 | 4592 | Missense Mutation | CCG,CTG | P,L 346 | XP_016873246.1 | |
XM_017017758.1 | 4592 | Missense Mutation | CCG,CTG | P,L 334 | XP_016873247.1 |