Colon Cancer: Gene >> IFIT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371811
Start	89338750:89338750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95G>T
AA Mutation	p.Arg32Met(p.R32M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371811
Start	89340012:89340012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1357A>G
AA Mutation	p.Ile453Val(p.I453V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371811
Start	89339035:89339035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380T>G
AA Mutation	p.Phe127Cys(p.F127C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371811
Start	89339749:89339749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1094G>A
AA Mutation	p.Cys365Tyr(p.C365Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371811
Start	89339949:89339949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371811
Start	89338781:89338781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.126T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371811
Start	89339120:89339120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34847428
CDS Mutation	c.465G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371811
Start	89339991:89339992(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1336_1337delCT
AA Mutation	p.Leu446LysfsTer16(p.L446Kfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371811
Start	89339822:89339823(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1173dupA
AA Mutation	p.Ser392IlefsTer3(p.S392Ifs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IFIT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371811
Start	89339289:89339289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634C>A
AA Mutation	p.Leu212Ile(p.L212I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371811
Start	89338821:89338821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.166T>G
AA Mutation	p.Leu56Val(p.L56V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript