Colon Cancer: Gene >> TRIM31

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376734
Start	30112672:30112672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134A>G
AA Mutation	p.Glu45Gly(p.E45G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376734
Start	30112552:30112552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254A>C
AA Mutation	p.Glu85Ala(p.E85A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376734
Start	30108112:30108112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824A>G
AA Mutation	p.Lys275Arg(p.K275R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376734
Start	30112756:30112756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50C>T
AA Mutation	p.Pro17Leu(p.P17L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376734
Start	30103651:30103651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1163C>T
AA Mutation	p.Ala388Val(p.A388V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376734
Start	30104115:30104115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1011G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM31

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376734
Start	30110470:30110470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722T>A
AA Mutation	p.Met241Lys(p.M241K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript