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Summary

Isoform:
Position:
14
Ref:
T
Mutation:
M
PTM impact:
direct
PTM affected:
4
Kinases:

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: 14T

Affected site:

Position: 14
Residue: T
Type: phosphorylation

Impact:

direct

Other known mutations affecting this site

Mutation In sequence Distance Impact
20Q ASTSRRFTPPSTA[L/Q]LS 6
distal
16S ASTSRRFTP[P/S]PSTALS 2
proximal
14M ASTSRRF[T/M]TPPSTALS 0
direct
12C ASTSR[R/C]RFTPPSTALS 2
network-rewiring
8R A[S/R]STSRRFTPPSTALS 6
distal
8N A[S/N]STSRRFTPPSTALS 6
distal
10I AST[S/I]SRRFTPPSTALS 4
distal

PTM Site: 17S

Affected site:

Position: 17
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
22L SRRFTPPSTALS[P/L]PGK 5
distal
22T SRRFTPPSTALS[P/T]PGK 5
distal
20Q SRRFTPPSTA[L/Q]LSPGK 3
distal
16S SRRFTP[P/S]PSTALSPGK 1
proximal
14M SRRF[T/M]TPPSTALSPGK 3
distal
12C SR[R/C]RFTPPSTALSPGK 5
network-rewiring

PTM Site: 18T

Affected site:

Position: 18
Residue: T
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
22L RRFTPPSTALS[P/L]PGKM 4
distal
22T RRFTPPSTALS[P/T]PGKM 4
distal
20Q RRFTPPSTA[L/Q]LSPGKM 2
proximal
16S RRFTP[P/S]PSTALSPGKM 2
proximal
14M RRF[T/M]TPPSTALSPGKM 4
distal
12C R[R/C]RFTPPSTALSPGKM 6
distal

PTM Site: 21S

Affected site:

Position: 21
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
26G TPPSTALSPGKM[S/G]SEA 5
distal
25I TPPSTALSPGK[M/I]MSEA 4
distal
25K TPPSTALSPGK[M/K]MSEA 4
distal
22L TPPSTALS[P/L]PGKMSEA 1
network-rewiring
22T TPPSTALS[P/T]PGKMSEA 1
network-rewiring
20Q TPPSTA[L/Q]LSPGKMSEA 1
proximal
16S TP[P/S]PSTALSPGKMSEA 5
distal

External references

dbSNP:

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