FMNL1 A694T

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Mutation:

Summary

Isoform:

NM_005892

Position:

694

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)

[0.6074]

Minor Allele Frequency: (1000 Genomes)

[0.638978]

PTM Site: 689S

Affected site:

Position: 689

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
692F	KTKSQGPSLD[L/F]LSALK	3	distal
694T	KTKSQGPSLDLS[A/T]ALK	5	distal

PTM Site: 693S

Affected site:

Position: 693

Residue: S

Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
692F	QGPSLD[L/F]LSALKSKAA	1	proximal
694T	QGPSLDLS[A/T]ALKSKAA	1	proximal

PTM Site: 696K

Affected site:

Position: 696

Residue: K

Type: ubiquitination

Impact:

proximal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
692F	SLD[L/F]LSALKSKAAQKA	4	distal
694T	SLDLS[A/T]ALKSKAAQKA	2	proximal

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