MINK1 P738L

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Mutation:

Summary

Isoform:

NM_170663

Position:

738

Ref:

Mutation:

PTM impact:

proximal

PTM affected:

Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

[48.8488]

Minor Allele Frequency: (1000 Genomes)

[70.028]

PTM Site: 735S

Affected site:

Position: 735

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
731L	ERN[R/L]RVGVSSKPDSSP	4	distal
732M	ERNR[V/M]VGVSSKPDSSP	3	distal
734A	ERNRVG[V/A]VSSKPDSSP	1	proximal
738L	ERNRVGVSSK[P/L]PDSSP	3	distal
731C	ERN[R/C]RVGVSSKPDSSP	4	distal

PTM Site: 740S

Affected site:

Position: 740

Residue: S

Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
734A	G[V/A]VSSKPDSSPVLSPG	6	distal
738L	GVSSK[P/L]PDSSPVLSPG	2	proximal

PTM Site: 741S

Affected site:

Position: 741

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
738L	VSSK[P/L]PDSSPVLSPGN	3	distal

PTM Site: 745S

Affected site:

Position: 745

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact

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