Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGTGGCCTCTCCTCCATCAAATGC[C/T]GTGTGGATGAGGACCTGGAGCCCAC
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 136131 | ||||||||||||||||||||||||||||||||
Literature Links: |
FMO4 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global - Not Available | Caucasian
|
CEPH (CEU) - Not Available | |||
EAS - Not Available | African American
|
YRI (Yoruba) - Not Available | |||
SAS - Not Available | Japanese
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CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Chinese
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JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
FMO4 - flavin containing monooxygenase 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002022.2 | 494 | Missense Mutation | CGT,TGT | R,C 21 | NP_002013.1 | |
XM_005245045.3 | 494 | Intron | XP_005245102.1 | |||
XM_005245046.3 | 494 | Missense Mutation | CGT,TGT | R,C 21 | XP_005245103.1 | |
XM_005245048.3 | 494 | Missense Mutation | CGT,TGT | R,C 21 | XP_005245105.1 | |
XM_006711243.3 | 494 | Missense Mutation | CGT,TGT | R,C 21 | XP_006711306.1 | |
XM_011509347.2 | 494 | Missense Mutation | CGT,TGT | R,C 21 | XP_011507649.1 | |
XM_011509348.2 | 494 | Intron | XP_011507650.1 | |||
XM_011509349.2 | 494 | Missense Mutation | CGT,TGT | R,C 21 | XP_011507651.1 |
Set Membership: |
DME Validated Inventoried |