Colon Cancer: Gene >> MIIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235332
Start	12030080:12030080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541833150
CDS Mutation	c.898C>T
AA Mutation	p.Arg300Trp(p.R300W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000235332
Start	12030057:12030057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.875C>T
AA Mutation	p.Pro292Leu(p.P292L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000235332
Start	12031780:12031780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143726942
CDS Mutation	c.1139G>A
AA Mutation	p.Arg380Gln(p.R380Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000235332
Start	12022212:12022212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232G>A
AA Mutation	p.Asp78Asn(p.D78N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000235332
Start	12022291:12022291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311A>G
AA Mutation	p.Glu104Gly(p.E104G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000235332
Start	12029101:12029101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779477951
CDS Mutation	c.616C>T
AA Mutation	p.Arg206Trp(p.R206W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235332
Start	12029070:12029070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MIIP

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235332
Start	12029274:12029274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.708C>T
Mutation Classification	Silent
Feature Type	Transcript