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CATCAGCTTACTAGTAGCCCTGAAG[A/G]TATTCTAATGGTAAGACATGAAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611246 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ADAL 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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ADAL - adenosine deaminase like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012969.3 | 387 | Missense Mutation | GAT,GGT | D,G 82 | NP_001012987.1 | |
NM_001159280.2 | 387 | Missense Mutation | GAT,GGT | D,G 82 | NP_001152752.1 | |
NM_001324364.1 | 387 | Missense Mutation | GAT,GGT | D,G 82 | NP_001311293.1 | |
NM_001324365.1 | 387 | Missense Mutation | GAT,GGT | D,G 82 | NP_001311294.1 | |
NM_001324366.1 | 387 | Missense Mutation | GAT,GGT | D,G 82 | NP_001311295.1 | |
NM_001324367.1 | 387 | Missense Mutation | GAT,GGT | D,G 82 | NP_001311296.1 | |
NM_001324368.1 | 387 | Missense Mutation | GAT,GGT | D,G 82 | NP_001311297.1 | |
XM_011521291.2 | 387 | Missense Mutation | GAT,GGT | D,G 82 | XP_011519593.1 | |
XM_017021964.1 | 387 | Missense Mutation | GAT,GGT | D,G 82 | XP_016877453.1 | |
XM_017021965.1 | 387 | Missense Mutation | GAT,GGT | D,G 82 | XP_016877454.1 | |
XM_017021966.1 | 387 | Missense Mutation | GAT,GGT | D,G 82 | XP_016877455.1 | |
XM_017021967.1 | 387 | Missense Mutation | GAT,GGT | D,G 47 | XP_016877456.1 | |
XM_017021968.1 | 387 | Missense Mutation | GAT,GGT | D,G 82 | XP_016877457.1 | |
XM_017021969.1 | 387 | Missense Mutation | GAT,GGT | D,G 82 | XP_016877458.1 |
LCMT2 - leucine carboxyl methyltransferase 2 | ||||||
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There are no transcripts associated with this gene. |