Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TATGGTGGGCAGGTGGGTTTCTGGA[A/T]CAAACTGTATAGCCTGCAAACAGAA
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 612779 | ||||||||||||||||||||||||||||||||
Literature Links: |
DPYD 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
|
CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Chinese
|
JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
DPYD - dihydropyrimidine dehydrogenase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000110.3 | 3268 | Missense Mutation | GAT,GTT | D,V 974 | NP_000101.2 | |
NM_001160301.1 | 3268 | Intron | NP_001153773.1 | |||
XM_005270562.3 | 3268 | Missense Mutation | GAT,GTT | D,V 902 | XP_005270619.2 | |
XM_006710397.3 | 3268 | Intron | XP_006710460.1 | |||
XM_017000507.1 | 3268 | Missense Mutation | GAT,GTT | D,V 937 | XP_016855996.1 | |
XM_017000508.1 | 3268 | Missense Mutation | GAT,GTT | D,V 809 | XP_016855997.1 | |
XM_017000509.1 | 3268 | Missense Mutation | GAT,GTT | D,V 809 | XP_016855998.1 | |
XM_017000510.1 | 3268 | Missense Mutation | GAT,GTT | D,V 809 | XP_016855999.1 |
Set Membership: |
DME Validated Inventoried |