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Mutation:
GRIN2A R920S
Summary
Clinical Information
Cancer types: (TCGA MC3)
LUSC
Cancer types: (PCAWG)
Lung-SCC
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 913S
Affected site:
Position: 913
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 918S | SMSNMNSSRMDS[P/S]PKR | 5 |
distal
|
| 917A | SMSNMNSSRMD[S/A]SPKR | 4 |
distal
|
| 915T | SMSNMNSSR[M/T]MDSPKR | 2 |
proximal
|
| 912C | SMSNMN[S/C]SSRMDSPKR | 1 |
proximal
|
| 910I | SMSN[M/I]MNSSRMDSPKR | 3 |
distal
|
PTM Site: 917S
Affected site:
Position: 917
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 922V | MNSSRMDSPKRA[A/V]ADF | 5 |
distal
|
| 918S | MNSSRMDS[P/S]PKRAADF | 1 |
network-rewiring
|
| 917A | MNSSRMD[S/A]SPKRAADF | 0 |
direct
|
| 915T | MNSSR[M/T]MDSPKRAADF | 2 |
proximal
|
| 912C | MN[S/C]SSRMDSPKRAADF | 5 |
distal
|
| 920S | MNSSRMDSPK[R/S]RAADF | 3 |
distal
|
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