ANKRD11 F852L

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Mutation:

Summary

Isoform:

NM_001256182

Position:

852

Ref:

Mutation:

PTM impact:

distal

PTM affected:

Kinases:

Clinical Information

Cancer types: (TCGA MC3)

BLCA

Cancer types: (PCAWG)

Bladder-TCC

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 846S

Affected site:

Position: 846

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
840W	D[R/W]RWFSDLSDSSFDFK	6	distal
840Q	D[R/Q]RWFSDLSDSSFDFK	6	distal
847N	DRWFSDLS[D/N]DSSFDFK	1	proximal
852L	DRWFSDLSDSSFD[F/L]FK	6	distal

PTM Site: 848S

Affected site:

Position: 848

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
847N	WFSDLS[D/N]DSSFDFKGE	1	proximal
852L	WFSDLSDSSFD[F/L]FKGE	4	distal

PTM Site: 849S

Affected site:

Position: 849

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
847N	FSDLS[D/N]DSSFDFKGED	2	network-rewiring
852L	FSDLSDSSFD[F/L]FKGED	3	distal

PTM Site: 857S

Affected site:

Position: 857

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
861L	FDFKGEDSWDS[P/L]PVTD	4	distal
860L	FDFKGEDSWD[S/L]SPVTD	3	distal
852L	FD[F/L]FKGEDSWDSPVTD	5	distal

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