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Mutation:
FGA V416M
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0077]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 412T
Affected site:
Position: 412
Residue: T
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 416M | PNNPDWGTFEE[V/M]VSGN | 4 |
distal
|
| 408L | PNN[P/L]PDWGTFEEVSGN | 4 |
distal
|
| 407H | PN[N/H]NPDWGTFEEVSGN | 5 |
distal
|
PTM Site: 421S
Affected site:
Position: 421
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 416M | EE[V/M]VSGNVSPGTRREY | 5 |
distal
|
| 423E | EEVSGNVSP[G/E]GTRREY | 2 |
proximal
|
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