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Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604054 MIM: 602170 | ||||||||||||||||||||||||||
Literature Links: |
ACAA1 PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese)
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EUR - Not Available | |||||
AMR - Not Available |
ACAA1 - acetyl-CoA acyltransferase 1 | ||||||
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There are no transcripts associated with this gene. |
MYD88 - myeloid differentiation primary response 88 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172566.1 | 443 | Missense Mutation | ATG,CTG | M,L 87 | NP_001166037.1 | |
NM_001172567.1 | 443 | Missense Mutation | ATG,CTG | M,L 87 | NP_001166038.1 | |
NM_001172568.1 | 443 | Missense Mutation | ATG,CTG | M,L 87 | NP_001166039.1 | |
NM_001172569.1 | 443 | Missense Mutation | ATG,CTG | M,L 87 | NP_001166040.1 | |
NM_002468.4 | 443 | Missense Mutation | ATG,CTG | M,L 87 | NP_002459.2 | |
XM_005265172.1 | 443 | Missense Mutation | ATG,CTG | M,L 87 | XP_005265229.1 | |
XM_006713170.1 | 443 | Missense Mutation | ATG,CTG | M,L 87 | XP_006713233.1 |
Set Membership: |
HapMap |