Colon Cancer: Gene >> CLK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316308
Start	178617365:178617365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454G>A
AA Mutation	p.Gly152Arg(p.G152R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316308
Start	178603925:178603925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224G>C
AA Mutation	p.Lys408Asn(p.K408N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316308
Start	178613514:178613514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.785A>G
AA Mutation	p.His262Arg(p.H262R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316308
Start	178612861:178612861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856G>A
AA Mutation	p.Asp286Asn(p.D286N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316308
Start	178613538:178613538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.761G>A
AA Mutation	p.Ser254Asn(p.S254N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316308
Start	178618724:178618724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316308
Start	178612429:178612429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56336368
CDS Mutation	c.1038C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316308
Start	178617360:178617360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000316308
Start	178613545:178613545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754G>T
AA Mutation	p.Glu252Ter(p.E252*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000316308
Start	178623266:178623266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.151G>T
AA Mutation	p.Glu51Ter(p.E51*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316308
Start	178613807:178613808(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.578dupA
AA Mutation	p.Asn193LysfsTer7(p.N193Kfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000316308
Start	178618663:178618664(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.276_277insTCCACTCAA
AA Mutation	p.Asp92_Ile93insSerThrGln(p.D92_I93insSTQ)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CLK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316308
Start	178618717:178618717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760777347
CDS Mutation	c.223G>A
AA Mutation	p.Glu75Lys(p.E75K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316308
Start	178603719:178603719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1344G>T
Mutation Classification	Silent
Feature Type	Transcript