Colon Cancer: Gene >> HRASLS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255695
Start	63560153:63560153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.50C>A
AA Mutation	p.Ser17Tyr(p.S17Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255695
Start	63553029:63553029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424G>T
AA Mutation	p.Gly142Cys(p.G142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255695
Start	63558628:63558628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151C>A
AA Mutation	p.Leu51Met(p.L51M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000255695
Start	63553020:63553020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433G>A
AA Mutation	p.Ala145Thr(p.A145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255695
Start	63560128:63560128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HRASLS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255695
Start	63552968:63552968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.485A>G
AA Mutation	p.Gln162Arg(p.Q162R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript