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GGTCTTCCCTCTCCACGCTTGTAGA[C/T]GGAGACGGCGTCCGCGCTGACACCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601481 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYO10 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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MYO10 - myosin X | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012334.2 | 5306 | Missense Mutation | ATC,GTC | I,V 1982 | NP_036466.2 | |
XM_005248306.4 | 5306 | Missense Mutation | ATC,GTC | I,V 1340 | XP_005248363.1 | |
XM_005248307.2 | 5306 | Missense Mutation | ATC,GTC | I,V 1339 | XP_005248364.1 | |
XM_006714475.2 | 5306 | Missense Mutation | ATC,GTC | I,V 1959 | XP_006714538.1 | |
XM_011514046.2 | 5306 | Missense Mutation | ATC,GTC | I,V 1339 | XP_011512348.1 |