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CACCTGTAGGTCCTCTCTTCACCCA[A/G]CCGCTGCAGTAGAGGCCTGAGAGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 103270 MIM: 138254 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FDXR 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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FDXR - ferredoxin reductase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258012.3 | 1336 | Silent Mutation | GGC,GGT | G,G 440 | NP_001244941.2 | |
NM_001258013.3 | 1336 | Silent Mutation | GGC,GGT | G,G 428 | NP_001244942.2 | |
NM_001258014.3 | 1336 | Silent Mutation | GGC,GGT | G,G 389 | NP_001244943.2 | |
NM_001258015.2 | 1336 | Silent Mutation | GGC,GGT | G,G 357 | NP_001244944.1 | |
NM_001258016.3 | 1336 | Silent Mutation | GGC,GGT | G,G 345 | NP_001244945.2 | |
NM_004110.5 | 1336 | Silent Mutation | GGC,GGT | G,G 403 | NP_004101.3 | |
NM_024417.4 | 1336 | Silent Mutation | GGC,GGT | G,G 397 | NP_077728.3 | |
XM_006721772.1 | 1336 | Silent Mutation | GGC,GGT | G,G 398 | XP_006721835.1 | |
XM_011524527.1 | 1336 | Silent Mutation | GGC,GGT | G,G 404 | XP_011522829.1 | |
XM_011524528.1 | 1336 | Silent Mutation | GGC,GGT | G,G 401 | XP_011522830.1 | |
XM_011524529.1 | 1336 | Silent Mutation | GGC,GGT | G,G 400 | XP_011522831.1 | |
XM_011524531.2 | 1336 | Silent Mutation | GGC,GGT | G,G 352 | XP_011522833.1 | |
XM_011524532.2 | 1336 | Silent Mutation | GGC,GGT | G,G 351 | XP_011522834.1 | |
XM_011524533.2 | 1336 | Silent Mutation | GGC,GGT | G,G 346 | XP_011522835.1 |
GRIN2C - glutamate ionotropic receptor NMDA type subunit 2C | ||||||
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There are no transcripts associated with this gene. |