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GGGTCGGCCCACACCAGGCACTGGC[C/T]GTTGCCCCACGCTGCGCTTCCTCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601480 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYO1F 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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MYO1F - myosin IF | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012335.3 | 3146 | Missense Mutation | CAG,CGG | Q,R 1027 | NP_036467.2 | |
XM_011528024.1 | 3146 | Missense Mutation | CAG,CGG | Q,R 1048 | XP_011526326.1 | |
XM_011528025.1 | 3146 | Missense Mutation | CAG,CGG | Q,R 1044 | XP_011526327.1 | |
XM_011528026.1 | 3146 | Missense Mutation | CAG,CGG | Q,R 1019 | XP_011526328.1 | |
XM_011528027.1 | 3146 | Missense Mutation | CAG,CGG | Q,R 1003 | XP_011526329.1 | |
XM_011528028.2 | 3146 | Intron | XP_011526330.1 | |||
XM_017026821.1 | 3146 | Missense Mutation | CAG,CGG | Q,R 1023 | XP_016882310.1 |
ZNF414 - zinc finger protein 414 | ||||||
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There are no transcripts associated with this gene. |