Colon Cancer: Gene >> TNFRSF13B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261652
Start	16952458:16952458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187G>A
AA Mutation	p.Ala63Thr(p.A63T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261652
Start	16939696:16939696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372816963
CDS Mutation	c.733G>A
AA Mutation	p.Ala245Thr(p.A245T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261652
Start	16940365:16940365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140781824
CDS Mutation	c.592C>T
AA Mutation	p.Arg198Cys(p.R198C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261652
Start	16939712:16939712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199603343
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261652
Start	16940386:16940386(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs748653062
CDS Mutation	c.571delG
AA Mutation	p.Asp191IlefsTer30(p.D191Ifs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF13B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261652
Start	16939555:16939555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874G>T
AA Mutation	p.Gly292Cys(p.G292C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261652
Start	16952540:16952540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200868537
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261652
Start	16940452:16940453(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.504dupG
AA Mutation	p.Leu169AlafsTer68(p.L169Afs*68)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript