Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCCACCTGCAGGAGGCCTACTGCG[A/C]GTATGCCATCATCCTCATGGCGCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604148 | ||||||||||||||||||||
Literature Links: |
SLC13A2 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 |
SLC13A2 - solute carrier family 13 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145975.1 | 449 | Missense Mutation | GAG,GCG | E,A 39 | NP_001139447.1 | |
NM_003984.3 | 449 | Missense Mutation | GAG,GCG | E,A 39 | NP_003975.1 | |
XM_006722165.2 | 449 | UTR 5 | XP_006722228.1 | |||
XM_011525450.2 | 449 | Missense Mutation | GAG,GCG | E,A 39 | XP_011523752.1 | |
XM_011525451.1 | 449 | UTR 5 | XP_011523753.1 | |||
XM_011525452.1 | 449 | Missense Mutation | GAG,GCG | E,A 39 | XP_011523754.1 | |
XM_011525453.2 | 449 | Missense Mutation | GAG,GCG | E,A 39 | XP_011523755.1 | |
XM_011525454.2 | 449 | Missense Mutation | GAG,GCG | E,A 39 | XP_011523756.1 |