Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCAGGTCCTGCAGCAGCATCTGGC[C/T]GGTGAGGAAGCTGTCAGTCATGGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 103270 MIM: 138254 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FDXR PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
FDXR - ferredoxin reductase | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258012.3 | 1397 | Missense Mutation | AGC,GGC | S,G 461 | NP_001244941.2 | |
NM_001258013.3 | 1397 | Missense Mutation | AGC,GGC | S,G 449 | NP_001244942.2 | |
NM_001258014.3 | 1397 | Missense Mutation | AGC,GGC | S,G 410 | NP_001244943.2 | |
NM_001258015.2 | 1397 | Missense Mutation | AGC,GGC | S,G 378 | NP_001244944.1 | |
NM_001258016.3 | 1397 | Missense Mutation | AGC,GGC | S,G 366 | NP_001244945.2 | |
NM_004110.5 | 1397 | Missense Mutation | AGC,GGC | S,G 424 | NP_004101.3 | |
NM_024417.4 | 1397 | Missense Mutation | AGC,GGC | S,G 418 | NP_077728.3 | |
XM_006721772.1 | 1397 | Missense Mutation | AGC,GGC | S,G 419 | XP_006721835.1 | |
XM_011524527.1 | 1397 | Missense Mutation | AGC,GGC | S,G 425 | XP_011522829.1 | |
XM_011524528.1 | 1397 | Missense Mutation | AGC,GGC | S,G 422 | XP_011522830.1 | |
XM_011524529.1 | 1397 | Missense Mutation | AGC,GGC | S,G 421 | XP_011522831.1 | |
XM_011524531.2 | 1397 | Missense Mutation | AGC,GGC | S,G 373 | XP_011522833.1 | |
XM_011524532.2 | 1397 | Missense Mutation | AGC,GGC | S,G 372 | XP_011522834.1 | |
XM_011524533.2 | 1397 | Missense Mutation | AGC,GGC | S,G 367 | XP_011522835.1 |
GRIN2C - glutamate ionotropic receptor NMDA type subunit 2C | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |