Colon Cancer: Gene >> IFNGR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290219
Start	33432762:33432762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750400339
CDS Mutation	c.770C>T
AA Mutation	p.Ser257Leu(p.S257L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290219
Start	33432333:33432333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369753667
CDS Mutation	c.718G>C
AA Mutation	p.Asp240His(p.D240H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290219
Start	33426948:33426948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477C>A
AA Mutation	p.Phe159Leu(p.F159L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290219
Start	33421620:33421620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760780330
CDS Mutation	c.347G>A
AA Mutation	p.Arg116Gln(p.R116Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290219
Start	33426936:33426936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.465C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290219
Start	33421612:33421612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290219
Start	33426985:33426985(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.520delT
AA Mutation	p.Cys174ValfsTer29(p.C174Vfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IFNGR2

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000290219
Start	33432762:33432762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770C>A
AA Mutation	p.Ser257Ter(p.S257*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript