Colon Cancer: Gene >> TRAF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247668
Start	136923950:136923950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1237G>A
AA Mutation	p.Val413Met(p.V413M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247668
Start	136898825:136898825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>A
AA Mutation	p.Glu29Lys(p.E29K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000247668
Start	136923963:136923963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539035155
CDS Mutation	c.1250C>T
AA Mutation	p.Pro417Leu(p.P417L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000247668
Start	136908152:136908152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780585355
CDS Mutation	c.449G>A
AA Mutation	p.Arg150His(p.R150H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000247668
Start	136920394:136920394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839C>T
AA Mutation	p.Ala280Val(p.A280V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000247668
Start	136909929:136909929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767031937
CDS Mutation	c.538G>A
AA Mutation	p.Glu180Lys(p.E180K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000247668
Start	136921134:136921134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057G>A
AA Mutation	p.Val353Ile(p.V353I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247668
Start	136925721:136925721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560077345
CDS Mutation	c.1326C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247668
Start	136920416:136920416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769972448
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000247668
Start	136900512:136900512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>T
AA Mutation	p.Glu120Ter(p.E120*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000247668
Start	136920363:136920363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.808C>T
AA Mutation	p.Gln270Ter(p.Q270*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRAF2

No Mutation Annotation!