Colon Cancer: Gene >> HRASLS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264735
Start	193255681:193255681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346T>C
AA Mutation	p.Tyr116His(p.Y116H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264735
Start	193255721:193255721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386T>C
AA Mutation	p.Phe129Ser(p.F129S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264735
Start	193263209:193263209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755206372
CDS Mutation	c.694C>T
AA Mutation	p.Arg232Cys(p.R232C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HRASLS

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000264735
Start	193263035:193263035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520C>T
AA Mutation	p.Gln174Ter(p.Q174*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000264735
Start	193263137:193263137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622G>T
AA Mutation	p.Glu208Ter(p.E208*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript