Colon Cancer: Gene >> CLDN16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264734
Start	190408413:190408413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692A>C
AA Mutation	p.Lys231Thr(p.K231T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264734
Start	190410005:190410005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.887C>G
AA Mutation	p.Ala296Gly(p.A296G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264734
Start	190404833:190404833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499C>A
AA Mutation	p.Leu167Ile(p.L167I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264734
Start	190402428:190402428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765256758
CDS Mutation	c.416C>T
AA Mutation	p.Ala139Val(p.A139V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264734
Start	190402398:190402398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762831659
CDS Mutation	c.386G>A
AA Mutation	p.Arg129His(p.R129H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264734
Start	190408435:190408435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772803074
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264734
Start	190388445:190388445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.324+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CLDN16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264734
Start	190388362:190388362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243C>A
AA Mutation	p.Phe81Leu(p.F81L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript