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TCTCATTACTCATAGCAGGAGCCCA[C/T]GAAGGGTAAGTGTAGAGGTCAAACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 606193 | ||||||||||||||||||||
Literature Links: |
SLC13A1 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 |
SLC13A1 - solute carrier family 13 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001324400.1 | 2278 | Silent Mutation | NP_001311329.1 | |||
NM_022444.3 | 2278 | Silent Mutation | NP_071889.2 | |||
XM_011516515.2 | 2278 | Silent Mutation | XP_011514817.1 | |||
XM_011516516.2 | 2278 | Silent Mutation | XP_011514818.1 | |||
XM_011516517.2 | 2278 | Silent Mutation | XP_011514819.1 | |||
XM_011516518.2 | 2278 | Intron | XP_011514820.1 | |||
XM_011516519.2 | 2278 | Intron | XP_011514821.1 | |||
XM_017012554.1 | 2278 | Silent Mutation | XP_016868043.1 | |||
XM_017012555.1 | 2278 | Intron | XP_016868044.1 |