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GCCTGGCCCAGGGCGAGCATCAGAG[A/G]GGGCTGCTTTGGCAGGTTCTGGGAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614031 | ||||||||||||||||||||
Literature Links: |
GFOD2 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 |
GFOD2 - glucose-fructose oxidoreductase domain containing 2 | ||||||
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There are no transcripts associated with this gene. |
RANBP10 - RAN binding protein 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320238.1 | 1389 | Missense Mutation | CCT,TCT | P,S 500 | NP_001307167.1 | |
NM_001320239.1 | 1389 | Missense Mutation | CCT,TCT | P,S 561 | NP_001307168.1 | |
NM_001320240.1 | 1389 | Missense Mutation | CCT,TCT | P,S 358 | NP_001307169.1 | |
NM_020850.2 | 1389 | Missense Mutation | CCT,TCT | P,S 587 | NP_065901.1 | |
XM_005256070.2 | 1389 | Missense Mutation | CCT,TCT | P,S 617 | XP_005256127.1 | |
XM_005256072.2 | 1389 | Missense Mutation | CCT,TCT | P,S 485 | XP_005256129.1 | |
XM_006721238.3 | 1389 | Missense Mutation | CCT,TCT | P,S 461 | XP_006721301.1 | |
XM_011523245.2 | 1389 | Missense Mutation | CCT,TCT | P,S 358 | XP_011521547.1 | |
XM_011523247.2 | 1389 | Missense Mutation | CCT,TCT | P,S 388 | XP_011521549.1 | |
XM_017023507.1 | 1389 | Missense Mutation | CCT,TCT | P,S 403 | XP_016878996.1 | |
XM_017023508.1 | 1389 | Missense Mutation | CCT,TCT | P,S 388 | XP_016878997.1 | |
XM_017023509.1 | 1389 | Missense Mutation | CCT,TCT | P,S 358 | XP_016878998.1 |