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Summary

Isoform:
Position:
366
Ref:
I
Mutation:
T
PTM impact:
proximal
PTM affected:
2
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Bloom syndrome, Hereditary cancer-predisposing syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

[0.0199681]

PTM Site: 359T

Affected site:

Position: 359
Residue: T
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
353V E[L/V]LNPETSTDCDARQI 6
distal
355R ELN[P/R]PETSTDCDARQI 4
distal
355L ELN[P/L]PETSTDCDARQI 4
distal
363T ELNPETSTDCD[A/T]ARQI 4
distal
363V ELNPETSTDCD[A/V]ARQI 4
distal
364K ELNPETSTDCDA[R/K]RQI 5
distal

PTM Site: 367S

Affected site:

Position: 367
Residue: S
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
363T DCD[A/T]ARQISLQQQLIH 4
distal
363V DCD[A/V]ARQISLQQQLIH 4
distal
364K DCDA[R/K]RQISLQQQLIH 3
network-rewiring
366L DCDARQ[I/L]ISLQQQLIH 1
proximal
366T DCDARQ[I/T]ISLQQQLIH 1
proximal
367N DCDARQI[S/N]SLQQQLIH 0
direct
369H DCDARQISL[Q/H]QQQLIH 2
proximal
373V DCDARQISLQQQL[I/V]IH 6
distal
373N DCDARQISLQQQL[I/N]IH 6
distal

External references

dbSNP:

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