Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604500 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYO19 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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MYO19 - myosin XIX | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033580.2 | 3240 | Intron | NP_001028752.1 | |||
NM_001163735.1 | 3240 | Missense Mutation | CTC,TTC | L,F 863 | NP_001157207.1 | |
NM_025109.5 | 3240 | Missense Mutation | CTC,TTC | L,F 663 | NP_079385.2 | |
XM_011525286.1 | 3240 | Missense Mutation | CTC,TTC | L,F 940 | XP_011523588.1 | |
XM_011525287.1 | 3240 | Missense Mutation | CTC,TTC | L,F 938 | XP_011523589.1 | |
XM_011525290.2 | 3240 | Missense Mutation | CTC,TTC | L,F 894 | XP_011523592.1 | |
XM_017025157.1 | 3240 | Missense Mutation | CTC,TTC | L,F 940 | XP_016880646.1 | |
XM_017025158.1 | 3240 | Missense Mutation | CTC,TTC | L,F 909 | XP_016880647.1 | |
XM_017025159.1 | 3240 | Missense Mutation | CTC,TTC | L,F 896 | XP_016880648.1 | |
XM_017025160.1 | 3240 | Intron | XP_016880649.1 | |||
XM_017025161.1 | 3240 | Missense Mutation | CTC,TTC | L,F 747 | XP_016880650.1 |
ZNHIT3 - zinc finger HIT-type containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281432.1 | 3240 | UTR 3 | NP_001268361.1 | |||
NM_001281433.1 | 3240 | Intron | NP_001268362.1 | |||
NM_001281434.1 | 3240 | Intron | NP_001268363.1 | |||
NM_004773.3 | 3240 | Intron | NP_004764.1 |
Set Membership: |
HapMap Validated |