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Mutation:
GLIPR2 E38K
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0154]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 33K
Affected site:
Position: 33
Residue: K
Type: ubiquitination
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
31I | VPPLK[L/I]LCKNLNREAQ | 2 |
proximal
|
38K | VPPLKLCKNLNR[E/K]EAQ | 5 |
distal
|
39S | VPPLKLCKNLNRE[A/S]AQ | 6 |
distal
|
33E | VPPLKLC[K/E]KNLNREAQ | 0 |
direct
|
37W | VPPLKLCKNLN[R/W]REAQ | 4 |
distal
|
37Q | VPPLKLCKNLN[R/Q]REAQ | 4 |
distal
|
PTM Site: 42Y
Affected site:
Position: 42
Residue: Y
Type: phosphorylation
Impact:
distalOther 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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