Colon Cancer: Gene >> TRAF7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326181
Start	2175912:2175912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1705A>G
AA Mutation	p.Asn569Asp(p.N569D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326181
Start	2173809:2173809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1108G>A
AA Mutation	p.Ala370Thr(p.A370T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326181
Start	2172317:2172317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.602C>T
AA Mutation	p.Pro201Leu(p.P201L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326181
Start	2173297:2173297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.910G>A
AA Mutation	p.Ala304Thr(p.A304T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326181
Start	2173812:2173812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111C>T
AA Mutation	p.Arg371Trp(p.R371W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326181
Start	2175554:2175554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1558A>T
AA Mutation	p.Asn520Tyr(p.N520Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000326181
Start	2176307:2176307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1921C>T
AA Mutation	p.Arg641Cys(p.R641C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000326181
Start	2172202:2172202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751318317
CDS Mutation	c.487G>A
AA Mutation	p.Val163Met(p.V163M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000326181
Start	2173483:2173483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144751745
CDS Mutation	c.1015G>A
AA Mutation	p.Val339Ile(p.V339I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000326181
Start	2171593:2171593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766294780
CDS Mutation	c.463G>A
AA Mutation	p.Ala155Thr(p.A155T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326181
Start	2171293:2171293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751636822
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326181
Start	2170646:2170646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200035101
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326181
Start	2176114:2176114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1812C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326181
Start	2175595:2175595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1599G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326181
Start	2176571:2176571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2010C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRAF7

No Mutation Annotation!