EPS15L1 P699S

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Mutation:

Summary

Isoform:

NM_001258374

Position:

699

Ref:

Mutation:

PTM impact:

proximal

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: 694K

Affected site:

Position: 694

Residue: K

Type: ubiquitination

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
689W	FT[S/W]SDPFTKNPSLPSK	5	distal
693M	FTSDPF[T/M]TKNPSLPSK	1	proximal
690Y	FTS[D/Y]DPFTKNPSLPSK	4	distal
699S	FTSDPFTKNPSL[P/S]PSK	5	distal
698F	FTSDPFTKNPS[L/F]LPSK	4	distal
689L	FT[S/L]SDPFTKNPSLPSK	5	distal

PTM Site: 697S

Affected site:

Position: 697

Residue: S

Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
701R	DPFTKNPSLPS[K/R]KLDP	4	distal
693M	DPF[T/M]TKNPSLPSKLDP	4	distal
699S	DPFTKNPSL[P/S]PSKLDP	2	proximal
698F	DPFTKNPS[L/F]LPSKLDP	1	proximal

PTM Site: 701K

Affected site:

Position: 701

Residue: K

Type: ubiquitination

Impact:

proximal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
701R	KNPSLPS[K/R]KLDPFESS	0	direct
699S	KNPSL[P/S]PSKLDPFESS	2	proximal
698F	KNPS[L/F]LPSKLDPFESS	3	distal
707C	KNPSLPSKLDPFE[S/C]SS	6	distal

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