Colon Cancer: Gene >> SRI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265729
Start	88219998:88219998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29G>T
AA Mutation	p.Gly10Val(p.G10V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265729
Start	88219999:88219999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28G>T
AA Mutation	p.Gly10Cys(p.G10C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265729
Start	88218883:88218883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776492181
CDS Mutation	c.111T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265729
Start	88209379:88209379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183967956
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SRI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265729
Start	88209410:88209410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748393938
CDS Mutation	c.440G>A
AA Mutation	p.Arg147Gln(p.R147Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265729
Start	88209381:88209381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754279084
CDS Mutation	c.469G>A
AA Mutation	p.Asp157Asn(p.D157N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript