Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TACCCCTTCGTTCTCACCATTCAGC[C/T]ACTGATAGGAGCCATCGCTGCAGGT
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609523 | ||||||||||||||||||||||||||||||||
Literature Links: |
ALDH3A2 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global - Not Available | Caucasian
|
CEPH (CEU) - Not Available | |||
EAS - Not Available | African American
|
YRI (Yoruba) - Not Available | |||
SAS - Not Available | Japanese
|
CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Chinese
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JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
ALDH3A2 - aldehyde dehydrogenase 3 family member A2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000382.2 | 491 | Missense Mutation | CCA,CTA | P,L 121 | NP_000373.1 | |
NM_001031806.1 | 491 | Missense Mutation | CCA,CTA | P,L 121 | NP_001026976.1 | |
XM_011523732.1 | 491 | Missense Mutation | CCA,CTA | P,L 121 | XP_011522034.1 | |
XM_011523733.1 | 491 | Missense Mutation | CCA,CTA | P,L 121 | XP_011522035.1 | |
XM_017024355.1 | 491 | Missense Mutation | CCA,CTA | P,L 121 | XP_016879844.1 | |
XM_017024356.1 | 491 | Missense Mutation | CCA,CTA | P,L 121 | XP_016879845.1 | |
XM_017024357.1 | 491 | Missense Mutation | CCA,CTA | P,L 121 | XP_016879846.1 | |
XM_017024358.1 | 491 | Missense Mutation | CCA,CTA | P,L 121 | XP_016879847.1 |
Set Membership: |
DME Validated Inventoried |