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Mutation:
TMEM200A P346A
Summary
Clinical Information
Cancer types: (TCGA MC3)
HNSC
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 350S
Affected site:
Position: 350
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 351T | TVLPRNNS[I/T]IGESLSS | 1 |
proximal
|
| 356L | TVLPRNNSIGESL[S/L]SS | 6 |
distal
|
| 350Y | TVLPRNN[S/Y]SIGESLSS | 0 |
direct
|
| 356T | TVLPRNNSIGESL[S/T]SS | 6 |
distal
|
| 352E | TVLPRNNSI[G/E]GESLSS | 2 |
proximal
|
| 346A | TVL[P/A]PRNNSIGESLSS | 4 |
distal
|
| 350F | TVLPRNN[S/F]SIGESLSS | 0 |
direct
|
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