Colon Cancer: Gene >> IFIT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89307206:89307206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250A>C
AA Mutation	p.Lys417Thr(p.K417T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89306707:89306707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537050168
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Cys(p.R251C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89306857:89306857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.901C>G
AA Mutation	p.Leu301Val(p.L301V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89306155:89306155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199A>C
AA Mutation	p.Asn67His(p.N67H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371826
Start	89306153:89306153(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.200delA
AA Mutation	p.Asn67ThrfsTer14(p.N67Tfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371826
Start	89306767:89306767(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.815delA
AA Mutation	p.Lys272ArgfsTer3(p.K272Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000371826
Start	89307220:89307220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773031617
CDS Mutation	c.1264C>T
AA Mutation	p.Arg422Ter(p.R422*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000371826
Start	89306767:89306767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770640915
CDS Mutation	c.811A>T
AA Mutation	p.Lys271Ter(p.K271*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IFIT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89306772:89306772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.816G>C
AA Mutation	p.Lys272Asn(p.K272N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89306466:89306466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>T
AA Mutation	p.Lys170Asn(p.K170N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89307141:89307141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1185T>G
AA Mutation	p.Phe395Leu(p.F395L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	start_lost;splice_region_variant
Transcription ID	ENST00000371826
Start	89302126:89302126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3G>T
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript