Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603475 MIM: 600044 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CHRD PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | ||||||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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CHRD - chordin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304472.1 | 687 | Silent Mutation | CCC,CCG | P,P 147 | NP_001291401.1 | |
NM_001304473.1 | 687 | UTR 5 | NP_001291402.1 | |||
NM_001304474.1 | 687 | UTR 5 | NP_001291403.1 | |||
NM_003741.3 | 687 | Silent Mutation | CCC,CCG | P,P 147 | NP_003732.2 | |
XM_011513254.1 | 687 | Silent Mutation | CCC,CCG | P,P 147 | XP_011511556.1 | |
XM_011513256.1 | 687 | UTR 5 | XP_011511558.1 | |||
XM_017007388.1 | 687 | Silent Mutation | CCC,CCG | P,P 147 | XP_016862877.1 | |
XM_017007389.1 | 687 | Silent Mutation | CCC,CCG | P,P 147 | XP_016862878.1 | |
XM_017007390.1 | 687 | Silent Mutation | CCC,CCG | P,P 147 | XP_016862879.1 | |
XM_017007391.1 | 687 | Silent Mutation | CCC,CCG | P,P 147 | XP_016862880.1 | |
XM_017007392.1 | 687 | Silent Mutation | CCC,CCG | P,P 147 | XP_016862881.1 | |
XM_017007393.1 | 687 | Silent Mutation | CCC,CCG | P,P 147 | XP_016862882.1 | |
XM_017007394.1 | 687 | UTR 5 | XP_016862883.1 |
THPO - thrombopoietin | ||||||
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There are no transcripts associated with this gene. |