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Mutation:
ATG9A A646V
Summary
Isoform:
Position:
646
Ref:
A
Mutation:
V
PTM impact:
proximal
PTM affected:
3
Kinases:
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: 642S
Affected site:
Position: 642
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 646V | LPRDLQGSRHR[A/V]AEVA | 4 |
distal
|
PTM Site: 645R
Affected site:
Position: 645
Residue: R
Type: methylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 646V | DLQGSRHR[A/V]AEVASAL | 1 |
proximal
|
PTM Site: 650S
Affected site:
Position: 650
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 646V | RHR[A/V]AEVASALRSFSP | 4 |
distal
|
| 652V | RHRAEVASA[L/V]LRSFSP | 2 |
proximal
|
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