Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGTGGCGCTCAGCATGGCCTCCGT[A/C]TCCGGCAGGATCTCGTTCTGGTTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605207 | ||||||||||||||||||||
Literature Links: |
CYP26B1 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 |
CYP26B1 - cytochrome P450 family 26 subfamily B member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001277742.1 | 1312 | Missense Mutation | GAG,GAT | E,D 428 | NP_001264671.1 | |
NM_019885.3 | 1312 | Missense Mutation | GAG,GAT | E,D 503 | NP_063938.1 | |
XM_005264433.4 | 1312 | Missense Mutation | GAG,GAT | E,D 445 | XP_005264490.1 | |
XM_011532988.1 | 1312 | Missense Mutation | GAG,GAT | E,D 312 | XP_011531290.1 |