Colon Cancer: Gene >> WSB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315436
Start	118043219:118043219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.341A>G
AA Mutation	p.His114Arg(p.H114R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315436
Start	118052439:118052439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.53C>A
AA Mutation	p.Pro18His(p.P18H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315436
Start	118043322:118043322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550650687
CDS Mutation	c.238C>T
AA Mutation	p.Arg80Trp(p.R80W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315436
Start	118038380:118038380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568A>G
AA Mutation	p.Ile190Val(p.I190V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315436
Start	118036416:118036416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755C>T
AA Mutation	p.Ala252Val(p.A252V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315436
Start	118052399:118052399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777807817
CDS Mutation	c.93C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315436
Start	118036403:118036403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748861369
CDS Mutation	c.768G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WSB2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315436
Start	118052345:118052345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755524304
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript