Colon Cancer: Gene >> TRAF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102870400:102870400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>A
AA Mutation	p.Glu67Lys(p.E67K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102905594:102905594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1517G>A
AA Mutation	p.Arg506His(p.R506H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102886216:102886216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540563941
CDS Mutation	c.598G>A
AA Mutation	p.Val200Met(p.V200M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102876446:102876446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491A>T
AA Mutation	p.Asp164Val(p.D164V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102889570:102889570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.662A>G
AA Mutation	p.His221Arg(p.H221R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102876403:102876403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.448C>T
AA Mutation	p.Arg150Cys(p.R150C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102870275:102870275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370955205
CDS Mutation	c.74G>T
AA Mutation	p.Arg25Leu(p.R25L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102891364:102891364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766G>A
AA Mutation	p.Ala256Thr(p.A256T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392745
Start	102905460:102905460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141356642
CDS Mutation	c.1383C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392745
Start	102886215:102886215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756602156
CDS Mutation	c.597C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392745
Start	102905466:102905466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752675828
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392745
Start	102905760:102905760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1683T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392745
Start	102905497:102905497(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1425delT
AA Mutation	p.Phe475LeufsTer20(p.F475Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392745
Start	102897288:102897289(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.854dupA
AA Mutation	p.Asn285LysfsTer13(p.N285Kfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TRAF3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000392745
Start	102876358:102876358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Val135Met(p.V135M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000392745
Start	102875651:102875651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>T
AA Mutation	p.Glu109Ter(p.E109*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript