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CCGGGTCAGCGGGGTCACCCCTCAG[C/G]ACATGGTGGGGGCCACACCATTTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610177 MIM: 604533 | ||||||||||||||||||||
Literature Links: |
AEN 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 |
AEN - apoptosis enhancing nuclease | ||||||
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There are no transcripts associated with this gene. |
ISG20 - interferon stimulated exonuclease gene 20 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303233.1 | 401 | Missense Mutation | CAC,GAC | H,D 63 | NP_001290162.1 | |
NM_001303234.1 | 401 | Missense Mutation | CAC,GAC | H,D 63 | NP_001290163.1 | |
NM_001303235.1 | 401 | Intron | NP_001290164.1 | |||
NM_001303236.1 | 401 | UTR 5 | NP_001290165.1 | |||
NM_001303237.1 | 401 | Missense Mutation | CAC,GAC | H,D 63 | NP_001290166.1 | |
NM_002201.5 | 401 | Missense Mutation | CAC,GAC | H,D 63 | NP_002192.2 | |
XM_005254899.2 | 401 | Missense Mutation | CAC,GAC | H,D 63 | XP_005254956.1 | |
XM_006720488.3 | 401 | Missense Mutation | CAC,GAC | H,D 63 | XP_006720551.1 | |
XM_011521521.2 | 401 | Intron | XP_011519823.1 | |||
XM_017022147.1 | 401 | UTR 5 | XP_016877636.1 | |||
XM_017022148.1 | 401 | Missense Mutation | CAC,GAC | H,D 63 | XP_016877637.1 |