BCLAF1 S209C

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Mutation:

Summary

Isoform:

NM_001077441

Position:

209

Ref:

Mutation:

PTM impact:

direct

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)

no data

Minor Allele Frequency: (1000 Genomes)

[49.8203]

PTM Site: 206S

Affected site:

Position: 206

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
210D	IDEFNKSSATS[G/D]GDIW	4	distal
210S	IDEFNKSSATS[G/S]GDIW	4	distal
209C	IDEFNKSSAT[S/C]SGDIW	3	distal
201K	ID[E/K]EFNKSSATSGDIW	5	distal

PTM Site: 208T

Affected site:

Position: 208

Residue: T

Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
214S	EFNKSSATSGDIW[P/S]PG	6	distal
210D	EFNKSSATS[G/D]GDIWPG	2	proximal
210S	EFNKSSATS[G/S]GDIWPG	2	proximal
209C	EFNKSSAT[S/C]SGDIWPG	1	proximal

PTM Site: 209S

Affected site:

Position: 209

Residue: S

Type: phosphorylation

Impact:

direct

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
214S	FNKSSATSGDIW[P/S]PGL	5	distal
210D	FNKSSATS[G/D]GDIWPGL	1	proximal
210S	FNKSSATS[G/S]GDIWPGL	1	proximal
209C	FNKSSAT[S/C]SGDIWPGL	0	direct

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