Colon Cancer: Gene >> IFIT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371804
Start	89402592:89402592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317A>G
AA Mutation	p.Tyr106Cys(p.Y106C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371804
Start	89403039:89403039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764G>A
AA Mutation	p.Arg255Gln(p.R255Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000371804
Start	89392717:89392717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5G>T
AA Mutation	p.Ser2Ile(p.S2I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371804
Start	89403453:89403453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139524521
CDS Mutation	c.1178A>T
AA Mutation	p.Lys393Ile(p.K393I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371804
Start	89402946:89402946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113869967
CDS Mutation	c.671C>T
AA Mutation	p.Ala224Val(p.A224V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371804
Start	89402672:89402672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376965843
CDS Mutation	c.397C>T
AA Mutation	p.Arg133Cys(p.R133C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371804
Start	89402452:89402452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371804
Start	89402347:89402347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149440394
CDS Mutation	c.72G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371804
Start	89403276:89403276(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1007delA
AA Mutation	p.Lys336SerfsTer9(p.K336Sfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IFIT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371804
Start	89403544:89403544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1269G>T
AA Mutation	p.Lys423Asn(p.K423N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371804
Start	89403537:89403537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1262C>A
AA Mutation	p.Ser421Tyr(p.S421Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371804
Start	89403358:89403358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083G>T
AA Mutation	p.Glu361Asp(p.E361D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript