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Mutation:
BRCA1 I429T
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
Hereditary cancer-predisposing syndrome, Hereditary breast and ovarian cancer syndrome
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 423S
Affected site:
Position: 423
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
429R | LNEVDEYSGSSEK[I/R]ID | 6 |
distal
|
429T | LNEVDEYSGSSEK[I/T]ID | 6 |
distal
|
424R | LNEVDEYS[G/R]GSSEKID | 1 |
proximal
|
424S | LNEVDEYS[G/S]GSSEKID | 1 |
proximal
|
422F | LNEVDE[Y/F]YSGSSEKID | 1 |
proximal
|
422C | LNEVDE[Y/C]YSGSSEKID | 1 |
proximal
|
422H | LNEVDE[Y/H]YSGSSEKID | 1 |
proximal
|
421G | LNEVD[E/G]EYSGSSEKID | 2 |
network-rewiring
|
421K | LNEVD[E/K]EYSGSSEKID | 2 |
network-rewiring
|
420G | LNEV[D/G]DEYSGSSEKID | 3 |
distal
|
420Y | LNEV[D/Y]DEYSGSSEKID | 3 |
distal
|
420H | LNEV[D/H]DEYSGSSEKID | 3 |
distal
|
420N | LNEV[D/N]DEYSGSSEKID | 3 |
distal
|
419G | LNE[V/G]VDEYSGSSEKID | 4 |
distal
|
419L | LNE[V/L]VDEYSGSSEKID | 4 |
distal
|
419I | LNE[V/I]VDEYSGSSEKID | 4 |
distal
|
418A | LN[E/A]EVDEYSGSSEKID | 5 |
distal
|
417K | L[N/K]NEVDEYSGSSEKID | 6 |
distal
|
417S | L[N/S]NEVDEYSGSSEKID | 6 |
distal
|
418D | LN[E/D]EVDEYSGSSEKID | 5 |
distal
|
PTM Site: 425S
Affected site:
Position: 425
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
431I | EVDEYSGSSEKID[L/I]LL | 6 |
distal
|
430G | EVDEYSGSSEKI[D/G]DLL | 5 |
distal
|
429R | EVDEYSGSSEK[I/R]IDLL | 4 |
distal
|
429T | EVDEYSGSSEK[I/T]IDLL | 4 |
distal
|
424R | EVDEYS[G/R]GSSEKIDLL | 1 |
proximal
|
424S | EVDEYS[G/S]GSSEKIDLL | 1 |
proximal
|
422F | EVDE[Y/F]YSGSSEKIDLL | 3 |
distal
|
422C | EVDE[Y/C]YSGSSEKIDLL | 3 |
distal
|
422H | EVDE[Y/H]YSGSSEKIDLL | 3 |
distal
|
421G | EVD[E/G]EYSGSSEKIDLL | 4 |
distal
|
421K | EVD[E/K]EYSGSSEKIDLL | 4 |
distal
|
420G | EV[D/G]DEYSGSSEKIDLL | 5 |
distal
|
420Y | EV[D/Y]DEYSGSSEKIDLL | 5 |
distal
|
420H | EV[D/H]DEYSGSSEKIDLL | 5 |
distal
|
420N | EV[D/N]DEYSGSSEKIDLL | 5 |
distal
|
419G | E[V/G]VDEYSGSSEKIDLL | 6 |
distal
|
419L | E[V/L]VDEYSGSSEKIDLL | 6 |
distal
|
419I | E[V/I]VDEYSGSSEKIDLL | 6 |
distal
|
PTM Site: 426S
Affected site:
Position: 426
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
432P | VDEYSGSSEKIDL[L/P]LA | 6 |
distal
|
432M | VDEYSGSSEKIDL[L/M]LA | 6 |
distal
|
431I | VDEYSGSSEKID[L/I]LLA | 5 |
distal
|
430G | VDEYSGSSEKI[D/G]DLLA | 4 |
distal
|
429R | VDEYSGSSEK[I/R]IDLLA | 3 |
distal
|
429T | VDEYSGSSEK[I/T]IDLLA | 3 |
distal
|
424R | VDEYS[G/R]GSSEKIDLLA | 2 |
network-rewiring
|
424S | VDEYS[G/S]GSSEKIDLLA | 2 |
proximal
|
422F | VDE[Y/F]YSGSSEKIDLLA | 4 |
distal
|
422C | VDE[Y/C]YSGSSEKIDLLA | 4 |
distal
|
422H | VDE[Y/H]YSGSSEKIDLLA | 4 |
distal
|
421G | VD[E/G]EYSGSSEKIDLLA | 5 |
distal
|
421K | VD[E/K]EYSGSSEKIDLLA | 5 |
distal
|
420G | V[D/G]DEYSGSSEKIDLLA | 6 |
distal
|
420Y | V[D/Y]DEYSGSSEKIDLLA | 6 |
distal
|
420H | V[D/H]DEYSGSSEKIDLLA | 6 |
distal
|
420N | V[D/N]DEYSGSSEKIDLLA | 6 |
distal
|
PTM Site: 428K
Affected site:
Position: 428
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
434N | EYSGSSEKIDLLA[S/N]SD | 6 |
distal
|
434G | EYSGSSEKIDLLA[S/G]SD | 6 |
distal
|
434R | EYSGSSEKIDLLA[S/R]SD | 6 |
distal
|
432P | EYSGSSEKIDL[L/P]LASD | 4 |
distal
|
432M | EYSGSSEKIDL[L/M]LASD | 4 |
distal
|
431I | EYSGSSEKID[L/I]LLASD | 3 |
distal
|
430G | EYSGSSEKI[D/G]DLLASD | 2 |
proximal
|
429R | EYSGSSEK[I/R]IDLLASD | 1 |
proximal
|
429T | EYSGSSEK[I/T]IDLLASD | 1 |
proximal
|
424R | EYS[G/R]GSSEKIDLLASD | 4 |
distal
|
424S | EYS[G/S]GSSEKIDLLASD | 4 |
distal
|
422F | E[Y/F]YSGSSEKIDLLASD | 6 |
distal
|
422C | E[Y/C]YSGSSEKIDLLASD | 6 |
distal
|
422H | E[Y/H]YSGSSEKIDLLASD | 6 |
distal
|
PTM Site: 434S
Affected site:
Position: 434
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
440S | EKIDLLASDPHEA[L/S]LI | 6 |
distal
|
439G | EKIDLLASDPHE[A/G]ALI | 5 |
distal
|
439S | EKIDLLASDPHE[A/S]ALI | 5 |
distal
|
439T | EKIDLLASDPHE[A/T]ALI | 5 |
distal
|
437R | EKIDLLASDP[H/R]HEALI | 3 |
distal
|
437P | EKIDLLASDP[H/P]HEALI | 3 |
distal
|
437Y | EKIDLLASDP[H/Y]HEALI | 3 |
distal
|
434N | EKIDLLA[S/N]SDPHEALI | 0 |
direct
|
434G | EKIDLLA[S/G]SDPHEALI | 0 |
direct
|
434R | EKIDLLA[S/R]SDPHEALI | 0 |
direct
|
432P | EKIDL[L/P]LASDPHEALI | 2 |
proximal
|
432M | EKIDL[L/M]LASDPHEALI | 2 |
proximal
|
431I | EKID[L/I]LLASDPHEALI | 3 |
distal
|
430G | EKI[D/G]DLLASDPHEALI | 4 |
distal
|
429R | EK[I/R]IDLLASDPHEALI | 5 |
network-rewiring
|
429T | EK[I/T]IDLLASDPHEALI | 5 |
distal
|
External references
dbSNP:
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