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Mutation:

TRIM29 S26N

Summary

Isoform:
NM_012101
Position:
26
Ref:
S
Mutation:
N
PTM impact:
direct
PTM affected:
5
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

STAD

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 21S

Affected site:

Position: 21
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
22T PEARDARS[P/T]PSGPSGS 1
network-rewiring
20G PEARDA[R/G]RSPSGPSGS 1
proximal
26N PEARDARSPSGP[S/N]SGS 5
distal
23L PEARDARSP[S/L]SGPSGS 2
proximal

PTM Site: 23S

Affected site:

Position: 23
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
22T ARDARS[P/T]PSGPSGSLE 1
proximal
20G ARDA[R/G]RSPSGPSGSLE 3
network-rewiring
26N ARDARSPSGP[S/N]SGSLE 3
distal
23L ARDARSP[S/L]SGPSGSLE 0
direct

PTM Site: 26S

Affected site:

Position: 26
Residue: S
Type: phosphorylation

Impact:

direct

Other known mutations affecting this site

Mutation In sequence Distance Impact
30K ARSPSGPSGSL[E/K]ENGT 4
distal
22T ARS[P/T]PSGPSGSLENGT 4
distal
20G A[R/G]RSPSGPSGSLENGT 6
distal
26N ARSPSGP[S/N]SGSLENGT 0
direct
23L ARSP[S/L]SGPSGSLENGT 3
distal

PTM Site: 28S

Affected site:

Position: 28
Residue: S
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
30K SPSGPSGSL[E/K]ENGTKA 2
network-rewiring
22T S[P/T]PSGPSGSLENGTKA 6
distal
26N SPSGP[S/N]SGSLENGTKA 2
proximal
23L SP[S/L]SGPSGSLENGTKA 5
distal

PTM Site: 33T

Affected site:

Position: 33
Residue: T
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
30K SGSL[E/K]ENGTKADGKDA 3
network-rewiring
39N SGSLENGTKADGK[D/N]DA 6
distal

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