CTNND1 D217N

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Mutation:

Summary

Isoform:

NM_001206883

Position:

217

Ref:

Mutation:

PTM impact:

proximal

PTM affected:

Kinases:

CSNK1E, PRKCE

Clinical Information

Cancer types: (TCGA MC3)

SKCM

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: 214S

Affected site:

Position: 214

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
216M	PQVRVGGSS[V/M]VDLHRF	2	proximal
220C	PQVRVGGSSVDLH[R/C]RF	6	distal
211I	PQVR[V/I]VGGSSVDLHRF	3	distal
210Q	PQV[R/Q]RVGGSSVDLHRF	4	distal
210W	PQV[R/W]RVGGSSVDLHRF	4	distal
217N	PQVRVGGSSV[D/N]DLHRF	3	distal
215T	PQVRVGGS[S/T]SVDLHRF	1	proximal

PTM Site: 215S

Affected site:

Position: 215

Residue: S

Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
216M	QVRVGGSS[V/M]VDLHRFH	1	proximal
220C	QVRVGGSSVDLH[R/C]RFH	5	distal
211I	QVR[V/I]VGGSSVDLHRFH	4	distal
210Q	QV[R/Q]RVGGSSVDLHRFH	5	distal
210W	QV[R/W]RVGGSSVDLHRFH	5	distal
217N	QVRVGGSSV[D/N]DLHRFH	2	proximal
215T	QVRVGGS[S/T]SVDLHRFH	0	direct

If you have any questions or feedback about this mutation: