Colon Cancer: Gene >> PTK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000542869
Start	63530087:63530087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773312243
CDS Mutation	c.1159C>T
AA Mutation	p.Pro387Ser(p.P387S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000542869
Start	63537196:63537196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119A>C
AA Mutation	p.Lys40Thr(p.K40T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000542869
Start	63532556:63532556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802G>A
AA Mutation	p.Ala268Thr(p.A268T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000542869
Start	63532526:63532526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770065818
CDS Mutation	c.832G>A
AA Mutation	p.Asp278Asn(p.D278N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542869
Start	63529551:63529551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55745805
CDS Mutation	c.1341C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542869
Start	63534954:63534954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771237415
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000542869
Start	63534950:63534950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340T>C
AA Mutation	p.Tyr114His(p.Y114H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript