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TTCTTGGGCAGTAGAACAGGTAATG[C/G]CAAGAGAAGCAGCTCCCACACCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610792 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC22A25 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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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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SLC22A25 - solute carrier family 22 member 25 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_199352.3 | 1472 | Missense Mutation | GCC,GGC | A,G 448 | NP_955384.3 | |
XM_017017684.1 | 1472 | Missense Mutation | GCC,GGC | A,G 478 | XP_016873173.1 | |
XM_017017685.1 | 1472 | Missense Mutation | GCC,GGC | A,G 478 | XP_016873174.1 | |
XM_017017686.1 | 1472 | Missense Mutation | GCC,GGC | A,G 478 | XP_016873175.1 | |
XM_017017687.1 | 1472 | Missense Mutation | GCC,GGC | A,G 448 | XP_016873176.1 | |
XM_017017688.1 | 1472 | Missense Mutation | GCC,GGC | A,G 378 | XP_016873177.1 | |
XM_017017689.1 | 1472 | Missense Mutation | GCC,GGC | A,G 367 | XP_016873178.1 | |
XM_017017690.1 | 1472 | Missense Mutation | GCC,GGC | A,G 353 | XP_016873179.1 | |
XM_017017691.1 | 1472 | Missense Mutation | GCC,GGC | A,G 353 | XP_016873180.1 | |
XM_017017692.1 | 1472 | Missense Mutation | GCC,GGC | A,G 306 | XP_016873181.1 | |
XM_017017693.1 | 1472 | Missense Mutation | GCC,GGC | A,G 282 | XP_016873182.1 | |
XM_017017694.1 | 1472 | Missense Mutation | GCC,GGC | A,G 280 | XP_016873183.1 | |
XM_017017695.1 | 1472 | Intron | XP_016873184.1 | |||
XM_017017696.1 | 1472 | Missense Mutation | GCC,GGC | A,G 217 | XP_016873185.1 |
Set Membership: |
HapMap |