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TGTACCAAAGAGGAAGTGGAGCGAC[C/T]GCTGCCCACCCGACAAAGGGTTTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601762 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CASP10 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 | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CASP10 - caspase 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206524.1 | 732 | Missense Mutation | CCG,CTG | P,L 105 | NP_001193453.1 | |
NM_001206542.1 | 732 | Missense Mutation | CCG,CTG | P,L 105 | NP_001193471.1 | |
NM_001230.4 | 732 | Missense Mutation | CCG,CTG | P,L 105 | NP_001221.2 | |
NM_001306083.1 | 732 | Missense Mutation | CCG,CTG | P,L 105 | NP_001293012.1 | |
NM_032974.4 | 732 | Missense Mutation | CCG,CTG | P,L 105 | NP_116756.2 | |
NM_032976.3 | 732 | Missense Mutation | CCG,CTG | P,L 105 | NP_116758.1 | |
NM_032977.3 | 732 | Missense Mutation | CCG,CTG | P,L 105 | NP_116759.2 | |
XM_005246907.2 | 732 | Missense Mutation | CCG,CTG | P,L 105 | XP_005246964.1 | |
XM_006712796.3 | 732 | UTR 5 | XP_006712859.1 | |||
XM_011511990.2 | 732 | Missense Mutation | CCG,CTG | P,L 105 | XP_011510292.1 |