Colon Cancer: Gene >> CLDN17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286808
Start	30166280:30166280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338G>T
AA Mutation	p.Arg113Met(p.R113M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286808
Start	30165980:30165980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781665299
CDS Mutation	c.638C>T
AA Mutation	p.Thr213Met(p.T213M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286808
Start	30166284:30166284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770504734
CDS Mutation	c.334G>A
AA Mutation	p.Glu112Lys(p.E112K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286808
Start	30166020:30166020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182327550
CDS Mutation	c.598C>T
AA Mutation	p.Pro200Ser(p.P200S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286808
Start	30166039:30166039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286808
Start	30166567:30166567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.51C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000286808
Start	30166452:30166452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148594408
CDS Mutation	c.166C>T
AA Mutation	p.Arg56Ter(p.R56*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CLDN17

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000286808
Start	30165990:30165990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377679902
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Ter(p.R210*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript