Colon Cancer: Gene >> TRIM72

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322122
Start	31224627:31224627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1306G>A
AA Mutation	p.Val436Met(p.V436M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322122
Start	31219313:31219313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511G>A
AA Mutation	p.Ala171Thr(p.A171T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322122
Start	31222861:31222861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775787122
CDS Mutation	c.775G>A
AA Mutation	p.Ala259Thr(p.A259T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322122
Start	31219387:31219387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.585G>T
AA Mutation	p.Glu195Asp(p.E195D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322122
Start	31224215:31224215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.894G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322122
Start	31219348:31219348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760762806
CDS Mutation	c.546C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322122
Start	31224617:31224617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1296C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322122
Start	31224329:31224329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1008G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322122
Start	31222852:31222852(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.770delC
AA Mutation	p.Pro257HisfsTer28(p.P257Hfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM72

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322122
Start	31219104:31219104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400C>T
AA Mutation	p.Pro134Ser(p.P134S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript