CTNND1 G236C

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Mutation:

Summary

Isoform:

NM_001206883

Position:

236

Ref:

Mutation:

PTM impact:

proximal

PTM affected:

Kinases:

Clinical Information

Cancer types: (TCGA MC3)

LUAD

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: 234S

Affected site:

Position: 234

Residue: S

Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
233H	GLEDDQ[R/H]RSMGYDDLD	1	proximal
236C	GLEDDQRSM[G/C]GYDDLD	2	proximal
239N	GLEDDQRSMGYD[D/N]DLD	5	distal

PTM Site: 237Y

Affected site:

Position: 237

Residue: Y

Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
233H	DDQ[R/H]RSMGYDDLDYGM	4	distal
236C	DDQRSM[G/C]GYDDLDYGM	1	proximal
239N	DDQRSMGYD[D/N]DLDYGM	2	proximal

PTM Site: 242Y

Affected site:

Position: 242

Residue: Y

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
245I	MGYDDLDYGM[M/I]MSDYG	3	distal
236C	M[G/C]GYDDLDYGMMSDYG	6	distal
239N	MGYD[D/N]DLDYGMMSDYG	3	distal
245L	MGYDDLDYGM[M/L]MSDYG	3	distal

If you have any questions or feedback about this mutation: