Colon Cancer: Gene >> TNFRSF1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000162749
Start	6329413:6329413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768168665
CDS Mutation	c.1267C>T
AA Mutation	p.Arg423Cys(p.R423C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000162749
Start	6334237:6334237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.47T>C
AA Mutation	p.Leu16Pro(p.L16P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000162749
Start	6334117:6334117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199961053
CDS Mutation	c.167C>T
AA Mutation	p.Ser56Leu(p.S56L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000162749
Start	6334216:6334216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68A>G
AA Mutation	p.Tyr23Cys(p.Y23C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000162749
Start	6329489:6329489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1191C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000162749
Start	6329947:6329947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000162749
Start	6334205:6334205(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.79delG
AA Mutation	p.Val27LeufsTer8(p.V27Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF1A

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000162749
Start	6333806:6333813(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.246_253delGGAGTGTG
AA Mutation	p.Cys84ArgfsTer52(p.C84Rfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000162749
Start	6334245:6334245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.40-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript