SAFB T439I

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Mutation:

Summary

Isoform:

NM_001201339

Position:

439

Ref:

Mutation:

PTM impact:

direct

PTM affected:

Kinases:

Clinical Information

Cancer types: (TCGA MC3)

KIRP

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: 436K

Affected site:

Position: 436

Residue: K

Type: acetylation, ubiquitination

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
439I	YGKVVGAKVV[T/I]TNARS	3	distal

PTM Site: 439T

Affected site:

Position: 439

Residue: T

Type: phosphorylation

Impact:

direct

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
445A	VVGAKVVTNARSP[G/A]GA	6	distal
439I	VVGAKVV[T/I]TNARSPGA	0	direct

PTM Site: 443S

Affected site:

Position: 443

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
445A	KVVTNARSP[G/A]GARCYG	2	proximal
439I	KVV[T/I]TNARSPGARCYG	4	distal

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