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Mutation:
ANKIB1 V899F
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
[0.0199681]
PTM Site: 898S
Affected site:
Position: 898
Residue: S
Type: phosphorylation
Impact:
proximalOther 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
|
PTM Site: 905S
Affected site:
Position: 905
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
899F | S[V/F]VPRNTDSPRAALSS | 6 |
distal
|
907W | SVPRNTDSP[R/W]RAALSS | 2 |
network-rewiring
|
900L | SV[P/L]PRNTDSPRAALSS | 5 |
distal
|
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