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CAGAAACCGGTAAAGGTTTTACCCA[A/G]CAAAGAGCCAAATGCAGTTGAAGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 126065 | ||||||||||||||||||||
Literature Links: |
CYP24A1 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 |
CYP24A1 - cytochrome P450 family 24 subfamily A member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000782.4 | 1837 | Silent Mutation | TGC,TGT | C,C 477 | NP_000773.2 | |
NM_001128915.1 | 1837 | Intron | NP_001122387.1 | |||
XM_005260304.4 | 1837 | Silent Mutation | TGC,TGT | C,C 477 | XP_005260361.1 | |
XM_017027691.1 | 1837 | Silent Mutation | TGC,TGT | C,C 477 | XP_016883180.1 | |
XM_017027692.1 | 1837 | Silent Mutation | TGC,TGT | C,C 477 | XP_016883181.1 | |
XM_017027693.1 | 1837 | Intron | XP_016883182.1 |