Colon Cancer: Gene >> IFI44

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370747
Start	78655082:78655082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563G>A
AA Mutation	p.Arg188Gln(p.R188Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370747
Start	78655452:78655452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769794841
CDS Mutation	c.781G>A
AA Mutation	p.Gly261Ser(p.G261S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370747
Start	78655085:78655085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.566T>A
AA Mutation	p.Ile189Asn(p.I189N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370747
Start	78659384:78659384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913C>A
AA Mutation	p.His305Asn(p.H305N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370747
Start	78662864:78662864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1274C>A
AA Mutation	p.Pro425His(p.P425H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370747
Start	78655451:78655451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372409962
CDS Mutation	c.780C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370747
Start	78650648:78650648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374094806
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370747
Start	78650431:78650431(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.240delT
AA Mutation	p.Phe80LeufsTer13(p.F80Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000370747
Start	78650643:78650643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556294601
CDS Mutation	c.448C>T
AA Mutation	p.Arg150Ter(p.R150*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IFI44

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370747
Start	78650649:78650649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777464454
CDS Mutation	c.454G>A
AA Mutation	p.Glu152Lys(p.E152K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370747
Start	78650486:78650486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291A>T
Mutation Classification	Silent
Feature Type	Transcript