Colon Cancer: Gene >> TNFRSF19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382258
Start	23668706:23668706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854C>T
AA Mutation	p.Ala285Val(p.A285V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382258
Start	23668885:23668885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767042376
CDS Mutation	c.1033A>G
AA Mutation	p.Thr345Ala(p.T345A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382258
Start	23615957:23615957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.271C>T
AA Mutation	p.Pro91Ser(p.P91S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382258
Start	23668896:23668896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1044T>A
AA Mutation	p.Asp348Glu(p.D348E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382258
Start	23668886:23668886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115520634
CDS Mutation	c.1034C>T
AA Mutation	p.Thr345Met(p.T345M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382258
Start	23668723:23668723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.871A>G
AA Mutation	p.Thr291Ala(p.T291A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000382258
Start	23615984:23615984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149498209
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Cys(p.R100C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000382258
Start	23659195:23659195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591T>G
AA Mutation	p.Phe197Leu(p.F197L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000382258
Start	23668693:23668693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841A>G
AA Mutation	p.Asn281Asp(p.N281D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000382258
Start	23615985:23615985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299G>A
AA Mutation	p.Arg100His(p.R100H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382258
Start	23668695:23668695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781345372
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382258
Start	23668924:23668924(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1075delG
AA Mutation	p.Ala359LeufsTer25(p.A359Lfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382258
Start	23659147:23659147(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.544delC
AA Mutation	p.Leu182CysfsTer129(p.L182Cfs*129)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382258
Start	23669042:23669043(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1190_1191insAAGACGTT
AA Mutation	p.Leu398ArgfsTer4(p.L398Rfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382258
Start	23668864:23668864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012A>G
AA Mutation	p.Asn338Asp(p.N338D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382258
Start	23660477:23660477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000382258
Start	23590149:23590149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.-34-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript