Colon Cancer: Gene >> TRIM63

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374272
Start	26058457:26058457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.764A>C
AA Mutation	p.Lys255Thr(p.K255T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374272
Start	26053914:26053914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030T>C
AA Mutation	p.Ser344Pro(p.S344P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374272
Start	26061282:26061282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385A>C
AA Mutation	p.Lys129Gln(p.K129Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374272
Start	26057231:26057231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.951C>G
AA Mutation	p.Asp317Glu(p.D317E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374272
Start	26058491:26058491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>A
AA Mutation	p.Ala244Thr(p.A244T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374272
Start	26066294:26066294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34009998
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374272
Start	26067450:26067450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.45G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374272
Start	26066363:26066363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM63

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374272
Start	26066359:26066359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241G>A
AA Mutation	p.Glu81Lys(p.E81K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript