Colon Cancer: Gene >> WNT2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369684
Start	112515026:112515026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335G>A
AA Mutation	p.Arg112His(p.R112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369684
Start	112517317:112517317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766318758
CDS Mutation	c.878G>A
AA Mutation	p.Arg293His(p.R293H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369684
Start	112516320:112516320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584G>A
AA Mutation	p.Gly195Asp(p.G195D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369684
Start	112517242:112517242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803G>A
AA Mutation	p.Arg268His(p.R268H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369684
Start	112520289:112520289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956G>A
AA Mutation	p.Gly319Asp(p.G319D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369684
Start	112516318:112516318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149716293
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000369684
Start	112520375:112520375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Ter(p.R348*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> WNT2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369684
Start	112515077:112515077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386G>C
AA Mutation	p.Gly129Ala(p.G129A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369684
Start	112520458:112520458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139266843
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000369684
Start	112514992:112514992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748702984
CDS Mutation	c.301C>T
AA Mutation	p.Arg101Ter(p.R101*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript