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Mutation:
TMEM200A I351T
Summary
Isoform:
Position:
351
Ref:
I
Mutation:
T
PTM impact:
proximal
PTM affected:
1
Kinases:
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.2999]
Minor Allele Frequency: (1000 Genomes)
[0.09984029999999999]
PTM Site: 350S
Affected site:
Position: 350
Residue: S
Type: phosphorylation
Impact:
proximalOther 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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