Colon Cancer: Gene >> SDCBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339987
Start	1312708:1312708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138600579
CDS Mutation	c.439C>T
AA Mutation	p.Arg147Cys(p.R147C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339987
Start	1312594:1312594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553C>T
AA Mutation	p.Arg185Trp(p.R185W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339987
Start	1313354:1313354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370C>T
AA Mutation	p.Arg124Trp(p.R124W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339987
Start	1312440:1312440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629G>T
AA Mutation	p.Gly210Val(p.G210V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339987
Start	1312453:1312453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762408353
CDS Mutation	c.616G>A
AA Mutation	p.Val206Met(p.V206M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339987
Start	1313375:1313375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>A
AA Mutation	p.Gly117Ser(p.G117S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339987
Start	1312616:1312616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751628959
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339987
Start	1310817:1310817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143026050
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SDCBP2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339987
Start	1313451:1313451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript