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Mutation:
RANGAP1 H170L
Summary
Isoform:
Position:
170
Ref:
H
Mutation:
L
PTM impact:
proximal
PTM affected:
1
Kinases:
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
Panc-AdenoCA
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 172K
Affected site:
Position: 172
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 171Q | ALTECH[R/Q]RKSSAQGKP | 1 |
proximal
|
| 168K | ALT[E/K]ECHRKSSAQGKP | 4 |
distal
|
| 178N | ALTECHRKSSAQG[K/N]KP | 6 |
distal
|
| 178R | ALTECHRKSSAQG[K/R]KP | 6 |
distal
|
| 170L | ALTEC[H/L]HRKSSAQGKP | 2 |
proximal
|
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