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AACAGTCTCCTTCCACAAAACCATG[C/G]CGTCGCTCAAATGTAGCACCGTCGT
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 |
---|---|---|
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 |
MYO19 - myosin XIX | ||||||
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There are no transcripts associated with this gene. |
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 | 77 | Missense Mutation | CCG,GCG | P,A 2 | NP_001268361.1 | |
NM_001281433.1 | 77 | Missense Mutation | CCG,GCG | P,A 2 | NP_001268362.1 | |
NM_001281434.1 | 77 | Missense Mutation | CCG,GCG | P,A 2 | NP_001268363.1 | |
NM_004773.3 | 77 | Missense Mutation | CCG,GCG | P,A 2 | NP_004764.1 |