Colon Cancer: Gene >> RIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311320
Start	66334054:66334054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1456C>A
AA Mutation	p.Leu486Met(p.L486M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311320
Start	66335443:66335443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511C>T
AA Mutation	p.His171Tyr(p.H171Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311320
Start	66332371:66332371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2257G>C
AA Mutation	p.Glu753Gln(p.E753Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311320
Start	66333287:66333287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757984197
CDS Mutation	c.1846C>T
AA Mutation	p.Arg616Cys(p.R616C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311320
Start	66334801:66334801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.998G>A
AA Mutation	p.Ser333Asn(p.S333N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311320
Start	66335057:66335057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141887009
CDS Mutation	c.742C>T
AA Mutation	p.Arg248Cys(p.R248C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311320
Start	66332415:66332415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2213A>G
AA Mutation	p.Asp738Gly(p.D738G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311320
Start	66332531:66332531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148553978
CDS Mutation	c.2097C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311320
Start	66334768:66334768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779921706
CDS Mutation	c.1031G>A
AA Mutation	p.Arg344Gln(p.R344Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311320
Start	66335057:66335057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141887009
CDS Mutation	c.742C>T
AA Mutation	p.Arg248Cys(p.R248C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript