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Summary

Isoform:
Position:
676
Ref:
W
Mutation:
R
PTM impact:
distal
PTM affected:
3
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Hereditary cancer-predisposing syndrome, Tuberous sclerosis 1

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 672K

Affected site:

Position: 672
Residue: K
Type: ubiquitination

Impact:

distal

PTM Site: 673S

Affected site:

Position: 673
Residue: S
Type: phosphorylation

Impact:

distal

PTM Site: 682S

Affected site:

Position: 682
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
686G DWTHFGGSPPS[D/G]DEIR 4
distal
686N DWTHFGGSPPS[D/N]DEIR 4
distal
684R DWTHFGGSP[P/R]PSDEIR 2
network-rewiring
684S DWTHFGGSP[P/S]PSDEIR 2
proximal
683R DWTHFGGS[P/R]PPSDEIR 1
network-rewiring
682P DWTHFGG[S/P]SPPSDEIR 0
direct
681S DWTHFG[G/S]GSPPSDEIR 1
proximal
680E DWTHF[G/E]GGSPPSDEIR 2
network-rewiring
680R DWTHF[G/R]GGSPPSDEIR 2
network-rewiring
678L DWT[H/L]HFGGSPPSDEIR 4
distal
678R DWT[H/R]HFGGSPPSDEIR 4
distal
678Y DWT[H/Y]HFGGSPPSDEIR 4
distal
677I DW[T/I]THFGGSPPSDEIR 5
distal
676R D[W/R]WTHFGGSPPSDEIR 6
distal

External references

dbSNP:

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