Colon Cancer: Gene >> TRIM17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295033
Start	228408589:228408589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046G>T
AA Mutation	p.Gly349Val(p.G349V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295033
Start	228415066:228415066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7G>A
AA Mutation	p.Ala3Thr(p.A3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295033
Start	228408637:228408637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998G>A
AA Mutation	p.Arg333Gln(p.R333Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295033
Start	228414888:228414888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.185G>A
AA Mutation	p.Cys62Tyr(p.C62Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295033
Start	228414760:228414760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313C>T
AA Mutation	p.Pro105Ser(p.P105S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295033
Start	228409181:228409181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874G>T
AA Mutation	p.Gly292Cys(p.G292C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295033
Start	228414927:228414927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146G>A
AA Mutation	p.Gly49Asp(p.G49D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295033
Start	228411160:228411160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141172871
CDS Mutation	c.542G>A
AA Mutation	p.Arg181Gln(p.R181Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295033
Start	228414764:228414764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764944857
CDS Mutation	c.309C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295033
Start	228409197:228409197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM17

No Mutation Annotation!