Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGTCGACAATAGGGCAAACACTGA[A/G]ACACAGAGTACAGCCTGTACAAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
3 submissions
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 612779 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DPYD 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
|
DPYD - dihydropyrimidine dehydrogenase | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000110.3 | 3324 | Missense Mutation | CTC,TTC | L,F 993 | NP_000101.2 | |
NM_001160301.1 | 3324 | Intron | NP_001153773.1 | |||
XM_005270562.3 | 3324 | Missense Mutation | CTC,TTC | L,F 921 | XP_005270619.2 | |
XM_006710397.3 | 3324 | Intron | XP_006710460.1 | |||
XM_017000507.1 | 3324 | Missense Mutation | CTC,TTC | L,F 956 | XP_016855996.1 | |
XM_017000508.1 | 3324 | Missense Mutation | CTC,TTC | L,F 828 | XP_016855997.1 | |
XM_017000509.1 | 3324 | Missense Mutation | CTC,TTC | L,F 828 | XP_016855998.1 | |
XM_017000510.1 | 3324 | Missense Mutation | CTC,TTC | L,F 828 | XP_016855999.1 |