Colon Cancer: Gene >> RFXANK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303088
Start	19198687:19198687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749859039
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Cys(p.R199C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303088
Start	19198668:19198668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303088
Start	19198114:19198115(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.451dupC
AA Mutation	p.His151ProfsTer30(p.H151Pfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RFXANK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303088
Start	19199177:19199177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655G>A
AA Mutation	p.Glu219Lys(p.E219K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript