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Mutation:
ATG9A Q662H
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0082]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 656S
Affected site:
Position: 656
Residue: S
Type: phosphorylation, phosphorylation (SARS-CoV-2)
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
662H | ASALRSFSPLQPG[Q/H]QA | 6 |
distal
|
659H | ASALRSFSPL[Q/H]QPGQA | 3 |
distal
|
652V | ASA[L/V]LRSFSPLQPGQA | 4 |
distal
|
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