Colon Cancer: Gene >> KLHL35

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000539798
Start	75425407:75425407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777338493
CDS Mutation	c.1360G>A
AA Mutation	p.Val454Ile(p.V454I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000539798
Start	75428559:75428559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.949C>T
AA Mutation	p.Pro317Ser(p.P317S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000539798
Start	75423718:75423719(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1536_1537delGG
AA Mutation	p.Glu513GlyfsTer17(p.E513Gfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000539798
Start	75423768:75423768(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1487delG
AA Mutation	p.Gly496ValfsTer3(p.G496Vfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KLHL35

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000539798
Start	75428544:75428544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964T>C
AA Mutation	p.Tyr322His(p.Y322H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript