Colon Cancer: Gene >> IFNGR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367739
Start	137198380:137198380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1121T>G
AA Mutation	p.Ile374Arg(p.I374R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367739
Start	137198234:137198234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1267A>G
AA Mutation	p.Ser423Gly(p.S423G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367739
Start	137203638:137203638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367739
Start	137198400:137198400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149761943
CDS Mutation	c.1101G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367739
Start	137200904:137200904(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.838delA
AA Mutation	p.Ser280AlafsTer2(p.S280Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367739
Start	137204499:137204499(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.379delA
AA Mutation	p.Ile127LeufsTer16(p.I127Lfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367739
Start	137203535:137203536(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.696dupA
AA Mutation	p.Glu233ArgfsTer9(p.E233Rfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367739
Start	137198048:137198049(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1436_1452dupATAGACCAACAGAAGAT
AA Mutation	p.Ser485IlefsTer15(p.S485Ifs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367739
Start	137198367:137198368(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1132_1133dupAG
AA Mutation	p.Ser378ArgfsTer6(p.S378Rfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IFNGR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367739
Start	137204388:137204388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146687518
CDS Mutation	c.490G>A
AA Mutation	p.Glu164Lys(p.E164K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367739
Start	137198159:137198159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146424575
CDS Mutation	c.1342G>A
AA Mutation	p.Val448Ile(p.V448I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript