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Mutation:
RUNX1 T219A
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
Familial platelet disorder with associated myeloid malignancy
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 212S
Affected site:
Position: 212
Residue: S
Type: phosphorylation, phosphorylation (SARS-CoV-2)
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
218S | RRTAMRVSPHHPA[P/S]PT | 6 |
distal
|
217T | RRTAMRVSPHHP[A/T]APT | 5 |
distal
|
213A | RRTAMRVS[P/A]PHHPAPT | 1 |
network-rewiring
|
211I | RRTAMR[V/I]VSPHHPAPT | 1 |
proximal
|
209I | RRTA[M/I]MRVSPHHPAPT | 3 |
distal
|
206H | R[R/H]RTAMRVSPHHPAPT | 6 |
distal
|
206C | R[R/C]RTAMRVSPHHPAPT | 6 |
distal
|
209V | RRTA[M/V]MRVSPHHPAPT | 3 |
distal
|
PTM Site: 219T
Affected site:
Position: 219
Residue: T
Type: phosphorylation
Impact:
directOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
223H | SPHHPAPTPNP[R/H]RASL | 4 |
distal
|
223C | SPHHPAPTPNP[R/C]RASL | 4 |
distal
|
221T | SPHHPAPTP[N/T]NPRASL | 2 |
proximal
|
220S | SPHHPAPT[P/S]PNPRASL | 1 |
network-rewiring
|
219M | SPHHPAP[T/M]TPNPRASL | 0 |
direct
|
219A | SPHHPAP[T/A]TPNPRASL | 0 |
direct
|
218S | SPHHPA[P/S]PTPNPRASL | 1 |
proximal
|
217T | SPHHP[A/T]APTPNPRASL | 2 |
proximal
|
213A | S[P/A]PHHPAPTPNPRASL | 6 |
distal
|
PTM Site: 223R
Affected site:
Position: 223
Residue: R
Type: methylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
228R | PAPTPNPRASLN[H/R]HST | 5 |
distal
|
228N | PAPTPNPRASLN[H/N]HST | 5 |
distal
|
223H | PAPTPNP[R/H]RASLNHST | 0 |
direct
|
223C | PAPTPNP[R/C]RASLNHST | 0 |
direct
|
221T | PAPTP[N/T]NPRASLNHST | 2 |
proximal
|
220S | PAPT[P/S]PNPRASLNHST | 3 |
distal
|
219M | PAP[T/M]TPNPRASLNHST | 4 |
distal
|
219A | PAP[T/A]TPNPRASLNHST | 4 |
distal
|
218S | PA[P/S]PTPNPRASLNHST | 5 |
distal
|
217T | P[A/T]APTPNPRASLNHST | 6 |
distal
|
229F | PAPTPNPRASLNH[S/F]ST | 6 |
distal
|
PTM Site: 225S
Affected site:
Position: 225
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
230I | PTPNPRASLNHS[T/I]TAF | 5 |
distal
|
228R | PTPNPRASLN[H/R]HSTAF | 3 |
distal
|
228N | PTPNPRASLN[H/N]HSTAF | 3 |
distal
|
223H | PTPNP[R/H]RASLNHSTAF | 2 |
network-rewiring
|
223C | PTPNP[R/C]RASLNHSTAF | 2 |
network-rewiring
|
221T | PTP[N/T]NPRASLNHSTAF | 4 |
distal
|
220S | PT[P/S]PNPRASLNHSTAF | 5 |
distal
|
219M | P[T/M]TPNPRASLNHSTAF | 6 |
distal
|
219A | P[T/A]TPNPRASLNHSTAF | 6 |
distal
|
229F | PTPNPRASLNH[S/F]STAF | 4 |
distal
|
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