Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCCGCCCCCAGAGCAGCCCCACGG[C/T]GGATGACCAGCTGTTTCACTGATAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609523 MIM: 609833 | ||||||||||||||||||||
Literature Links: |
ALDH3A2 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 |
ALDH3A2 - aldehyde dehydrogenase 3 family member A2 | ||||||
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There are no transcripts associated with this gene. |
SLC47A2 - solute carrier family 47 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099646.1 | 1905 | Missense Mutation | CAC,CGC | H,R 541 | NP_001093116.1 | |
NM_001256663.1 | 1905 | Missense Mutation | CAC,CGC | H,R 555 | NP_001243592.1 | |
NM_152908.3 | 1905 | Missense Mutation | CAC,CGC | H,R 577 | NP_690872.2 | |
XM_017024221.1 | 1905 | Missense Mutation | CAC,CGC | H,R 591 | XP_016879710.1 | |
XM_017024222.1 | 1905 | Missense Mutation | CAC,CGC | H,R 542 | XP_016879711.1 | |
XM_017024223.1 | 1905 | Intron | XP_016879712.1 | |||
XM_017024224.1 | 1905 | Intron | XP_016879713.1 | |||
XM_017024225.1 | 1905 | Intron | XP_016879714.1 | |||
XM_017024226.1 | 1905 | Intron | XP_016879715.1 |