Colon Cancer: Gene >> FOLR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312293
Start	72192216:72192216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43T>C
AA Mutation	p.Trp15Arg(p.W15R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312293
Start	72195395:72195395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764420714
CDS Mutation	c.293G>A
AA Mutation	p.Arg98Gln(p.R98Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312293
Start	72195951:72195951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.548C>A
AA Mutation	p.Pro183His(p.P183H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312293
Start	72196109:72196109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.706G>A
AA Mutation	p.Ala236Thr(p.A236T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312293
Start	72195647:72195647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61735636
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FOLR1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000312293
Start	72195390:72195390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288C>A
AA Mutation	p.Cys96Ter(p.C96*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript