Colon Cancer: Gene >> CLCF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312438
Start	67365450:67365450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761887384
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Cys(p.R122C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312438
Start	67367471:67367471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172G>A
AA Mutation	p.Ala58Thr(p.A58T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312438
Start	67367612:67367613(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.30dupG
AA Mutation	p.Met11AspfsTer35(p.M11Dfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CLCF1

No Mutation Annotation!