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TGCCGCAGGGCTCATCCCCACCAGC[A/G]GAGGAGATATTCGTAGCTGAGGAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610825 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC25A45 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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SLC25A45 - solute carrier family 25 member 45 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077241.2 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | NP_001070709.2 | |
NM_001278250.2 | 1862 | Missense Mutation | CGC,TGC | R,C 261 | NP_001265179.2 | |
NM_001278251.2 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | NP_001265180.2 | |
NM_001300820.1 | 1862 | Missense Mutation | CGC,TGC | R,C 223 | NP_001287749.1 | |
NM_182556.3 | 1862 | Missense Mutation | CGC,TGC | R,C 285 | NP_872362.3 | |
XM_006718509.3 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_006718572.1 | |
XM_006718510.3 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_006718573.1 | |
XM_011544943.2 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_011543245.1 | |
XM_011544944.2 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_011543246.1 | |
XM_011544947.2 | 1862 | Intron | XP_011543249.1 | |||
XM_011544949.2 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_011543251.1 | |
XM_017017562.1 | 1862 | Intron | XP_016873051.1 | |||
XM_017017563.1 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_016873052.1 | |
XM_017017564.1 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_016873053.1 | |
XM_017017565.1 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_016873054.1 | |
XM_017017566.1 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_016873055.1 | |
XM_017017567.1 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_016873056.1 | |
XM_017017568.1 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_016873057.1 | |
XM_017017569.1 | 1862 | Missense Mutation | CGC,TGC | R,C 243 | XP_016873058.1 | |
XM_017017570.1 | 1862 | Missense Mutation | CGC,TGC | R,C 181 | XP_016873059.1 | |
XM_017017571.1 | 1862 | Missense Mutation | CGC,TGC | R,C 181 | XP_016873060.1 |