Colon Cancer: Gene >> CLDN11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000064724
Start	170432653:170432653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521T>A
AA Mutation	p.Val174Asp(p.V174D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000064724
Start	170423290:170423290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.354G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000064724
Start	170419099:170419099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000064724
Start	170419294:170419294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CLDN11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000064724
Start	170432532:170432532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143763226
CDS Mutation	c.400G>A
AA Mutation	p.Ala134Thr(p.A134T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript