Colon Cancer: Gene >> PLEKHA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000449726
Start	30052848:30052848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.778A>G
AA Mutation	p.Thr260Ala(p.T260A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000449726
Start	30061918:30061918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1120A>G
AA Mutation	p.Thr374Ala(p.T374A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000449726
Start	30054759:30054759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847G>T
AA Mutation	p.Asp283Tyr(p.D283Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000449726
Start	30050447:30050447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611T>G
AA Mutation	p.Ile204Ser(p.I204S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000449726
Start	30078747:30078747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1520T>G
AA Mutation	p.Leu507Ter(p.L507*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PLEKHA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000449726
Start	30052766:30052766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696G>T
AA Mutation	p.Glu232Asp(p.E232D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000449726
Start	30054838:30054838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.926C>A
AA Mutation	p.Pro309Gln(p.P309Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript