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Mutation:
GLIPR2 S43P
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0231]
Minor Allele Frequency: (1000 Genomes)
[0.0199681]
PTM Site: 42Y
Affected site:
Position: 42
Residue: Y
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 38K | LNR[E/K]EAQQYSEALAST | 4 |
distal
|
| 39S | LNRE[A/S]AQQYSEALAST | 3 |
distal
|
| 41E | LNREAQ[Q/E]QYSEALAST | 1 |
proximal
|
| 43P | LNREAQQY[S/P]SEALAST | 1 |
proximal
|
| 37W | LN[R/W]REAQQYSEALAST | 5 |
distal
|
| 37Q | LN[R/Q]REAQQYSEALAST | 5 |
distal
|
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