MINK1 V771A

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Mutation:

Summary

Isoform:

NM_153827

Position:

771

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)

[47.0885]

Minor Allele Frequency: (1000 Genomes)

[70.6669]

PTM Site: 772S

Affected site:

Position: 772

Residue: S

Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
768L	ERN[R/L]RVGVSSKPDSSP	4	distal
769M	ERNR[V/M]VGVSSKPDSSP	3	distal
771A	ERNRVG[V/A]VSSKPDSSP	1	proximal
775L	ERNRVGVSSK[P/L]PDSSP	3	distal
768C	ERN[R/C]RVGVSSKPDSSP	4	distal

PTM Site: 777S

Affected site:

Position: 777

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
771A	G[V/A]VSSKPDSSPVLSPG	6	distal
775L	GVSSK[P/L]PDSSPVLSPG	2	proximal

PTM Site: 778S

Affected site:

Position: 778

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
775L	VSSK[P/L]PDSSPVLSPGN	3	distal

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