Colon Cancer: Gene >> TRIM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6449164:6449164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2099G>A
AA Mutation	p.Gly700Asp(p.G700D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456125:6456125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1480G>A
AA Mutation	p.Ala494Thr(p.A494T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456873:6456873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.853G>A
AA Mutation	p.Ala285Thr(p.A285T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6451309:6451309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773436993
CDS Mutation	c.1663C>T
AA Mutation	p.Arg555Cys(p.R555C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456704:6456704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022C>T
AA Mutation	p.Ala341Val(p.A341V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456350:6456350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1376C>A
AA Mutation	p.Thr459Lys(p.T459K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456615:6456615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111G>A
AA Mutation	p.Gly371Ser(p.G371S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456668:6456668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757648121
CDS Mutation	c.1058G>A
AA Mutation	p.Arg353Gln(p.R353Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6457795:6457795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416G>A
AA Mutation	p.Arg139His(p.R139H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456659:6456659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373824947
CDS Mutation	c.1067G>A
AA Mutation	p.Arg356His(p.R356H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456810:6456810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Trp(p.R306W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456786:6456786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752724316
CDS Mutation	c.940G>A
AA Mutation	p.Ala314Thr(p.A314T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456962:6456962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764C>T
AA Mutation	p.Ala255Val(p.A255V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456558:6456558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168T>C
AA Mutation	p.Tyr390His(p.Y390H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456608:6456608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118G>A
AA Mutation	p.Arg373His(p.R373H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6457002:6457002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763067089
CDS Mutation	c.724C>T
AA Mutation	p.Arg242Cys(p.R242C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345851
Start	6458137:6458137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345851
Start	6458239:6458239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770797841
CDS Mutation	c.189G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6449041:6449041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148786669
CDS Mutation	c.2222G>A
AA Mutation	p.Arg741His(p.R741H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456390:6456390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336C>T
AA Mutation	p.Arg446Cys(p.R446C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6449175:6449175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2088C>A
AA Mutation	p.Phe696Leu(p.F696L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345851
Start	6456940:6456940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786C>A
Mutation Classification	Silent
Feature Type	Transcript