Colon Cancer: Gene >> IFNAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270139
Start	33355461:33355461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1586C>T
AA Mutation	p.Ser529Phe(p.S529F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270139
Start	33343349:33343349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.458G>A
AA Mutation	p.Ser153Asn(p.S153N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270139
Start	33349514:33349514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1114A>G
AA Mutation	p.Ile372Val(p.I372V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270139
Start	33352884:33352884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541858922
CDS Mutation	c.1270G>T
AA Mutation	p.Ala424Ser(p.A424S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270139
Start	33343570:33343570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567T>G
AA Mutation	p.Ile189Met(p.I189M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270139
Start	33355454:33355454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579T>G
AA Mutation	p.Tyr527Asp(p.Y527D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270139
Start	33343559:33343559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.556A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270139
Start	33335548:33335548(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.105delA
AA Mutation	p.Val36Ter(p.V36*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270139
Start	33335626:33335627(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.184dupT
AA Mutation	p.Ser62PhefsTer11(p.S62Ffs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IFNAR1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270139
Start	33349217:33349217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000270139
Start	33340998:33340998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript