Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACTCTTTCAGTGGTGGGCATCTGC[A/G]CTCTACCATCTGGCTGCTCAAATGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147678 MIM: 602665 | ||||||||||||||||||||
Literature Links: |
CASP1 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 |
CASP1 - caspase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001223.4 | 1132 | Missense Mutation | GCG,GTG | A,V 363 | NP_001214.1 | |
NM_001257118.2 | 1132 | Missense Mutation | GCG,GTG | A,V 384 | NP_001244047.1 | |
NM_001257119.2 | 1132 | Missense Mutation | GCG,GTG | A,V 363 | NP_001244048.1 | |
NM_033292.3 | 1132 | Missense Mutation | GCG,GTG | A,V 384 | NP_150634.1 | |
NM_033293.3 | 1132 | Missense Mutation | GCG,GTG | A,V 291 | NP_150635.1 | |
NM_033294.3 | 1132 | Missense Mutation | GCG,GTG | A,V 243 | NP_150636.1 | |
NM_033295.3 | 1132 | Missense Mutation | GCG,GTG | A,V 68 | NP_150637.1 | |
XM_017018393.1 | 1132 | Missense Mutation | GCG,GTG | A,V 381 | XP_016873882.1 | |
XM_017018394.1 | 1132 | Missense Mutation | GCG,GTG | A,V 381 | XP_016873883.1 | |
XM_017018395.1 | 1132 | Missense Mutation | GCG,GTG | A,V 360 | XP_016873884.1 | |
XM_017018396.1 | 1132 | Missense Mutation | GCG,GTG | A,V 354 | XP_016873885.1 |
CASP5 - caspase 5 | ||||||
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There are no transcripts associated with this gene. |