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Summary

Isoform:
Position:
897
Ref:
D
Mutation:
H
PTM impact:
proximal
PTM affected:
2
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

BLCA

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: 891S

Affected site:

Position: 891
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
887V SLG[A/V]AIGTSLPSRLDS 4
distal
897H SLGAIGTSLPSRL[D/H]DS 6
distal

PTM Site: 898S

Affected site:

Position: 898
Residue: S
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
899F SLPSRLDS[V/F]VPRNTDS 1
proximal
900L SLPSRLDSV[P/L]PRNTDS 2
proximal
897H SLPSRL[D/H]DSVPRNTDS 1
proximal

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