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CACCAGCTGCGGTGGTAGCAGTGGG[A/G]TTTGTGCTTCTTATGTTACCCAGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601761 | ||||||||||||||||||||
Literature Links: |
CASP7 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 |
CASP7 - caspase 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001227.4 | 67 | Intron | NP_001218.1 | |||
NM_001267056.1 | 67 | Intron | NP_001253985.1 | |||
NM_001267057.1 | 67 | Intron | NP_001253986.1 | |||
NM_001267058.1 | 67 | Intron | NP_001253987.1 | |||
NM_001320911.1 | 67 | Intron | NP_001307840.1 | |||
NM_033338.5 | 67 | Missense Mutation | ATT,GTT | I,V 26 | NP_203124.1 | |
NM_033339.4 | 67 | UTR 5 | NP_203125.1 | |||
NM_033340.3 | 67 | Intron | NP_203126.1 | |||
XM_006718017.3 | 67 | UTR 5 | XP_006718080.1 | |||
XM_011540260.1 | 67 | Intron | XP_011538562.1 | |||
XM_017016763.1 | 67 | Intron | XP_016872252.1 | |||
XM_017016764.1 | 67 | Intron | XP_016872253.1 |