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TCCTAGAAAAGTAAAATATGACTAA[A/C]AGCAATGGAGAAGAGCCCAAGATGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600111 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC1A3 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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SLC1A3 - solute carrier family 1 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166695.2 | 234 | Missense Mutation | AAA,AAC | K,N 3 | NP_001160167.1 | |
NM_001166696.2 | 234 | Missense Mutation | AAA,AAC | K,N 3 | NP_001160168.1 | |
NM_001289939.1 | 234 | Missense Mutation | AAA,AAC | K,N 3 | NP_001276868.1 | |
NM_001289940.1 | 234 | Missense Mutation | AAA,AAC | K,N 3 | NP_001276869.1 | |
NM_004172.4 | 234 | Missense Mutation | AAA,AAC | K,N 3 | NP_004163.3 | |
XM_005248342.2 | 234 | Missense Mutation | AAA,AAC | K,N 3 | XP_005248399.1 | |
XM_011514084.2 | 234 | UTR 5 | XP_011512386.1 |