Colon Cancer: Gene >> RD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367002
Start	211479151:211479151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473G>A
AA Mutation	p.Arg158His(p.R158H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367002
Start	211481184:211481184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755218137
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Trp(p.R78W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367002
Start	211481283:211481283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369960606
CDS Mutation	c.133C>T
AA Mutation	p.Arg45Trp(p.R45W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367002
Start	211479101:211479101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523C>T
AA Mutation	p.Arg175Trp(p.R175W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367002
Start	211479187:211479187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437C>T
AA Mutation	p.Pro146Leu(p.P146L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367002
Start	211479154:211479154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470C>T
AA Mutation	p.Ala157Val(p.A157V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367002
Start	211479234:211479234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367002
Start	211479144:211479144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.480G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367002
Start	211479145:211479145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778700426
CDS Mutation	c.479C>T
AA Mutation	p.Ser160Leu(p.S160L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript