Colon Cancer: Gene >> TRAF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373887
Start	120923724:120923724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759221945
CDS Mutation	c.209G>A
AA Mutation	p.Arg70His(p.R70H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373887
Start	120909306:120909306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.956G>A
AA Mutation	p.Arg319Lys(p.R319K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373887
Start	120909308:120909308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.954G>T
AA Mutation	p.Lys318Asn(p.K318N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373887
Start	120923708:120923708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225G>T
AA Mutation	p.Glu75Asp(p.E75D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373887
Start	120913450:120913450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560261396
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Cys(p.R195C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373887
Start	120923743:120923743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.190T>C
AA Mutation	p.Ser64Pro(p.S64P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373887
Start	120905062:120905062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138123440
CDS Mutation	c.1209C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373887
Start	120905200:120905200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377159992
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373887
Start	120913661:120913661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373887
Start	120911394:120911395(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.824dupA
AA Mutation	p.Asn275LysfsTer8(p.N275Kfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TRAF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373887
Start	120905070:120905070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371039591
CDS Mutation	c.1201G>A
AA Mutation	p.Val401Met(p.V401M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373887
Start	120923718:120923718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200495625
CDS Mutation	c.215G>A
AA Mutation	p.Arg72Gln(p.R72Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript