Colon Cancer: Gene >> CLDN6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328796
Start	3015756:3015756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266T>G
AA Mutation	p.Leu89Arg(p.L89R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328796
Start	3015364:3015364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150318164
CDS Mutation	c.658G>A
AA Mutation	p.Val220Ile(p.V220I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328796
Start	3015825:3015825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197T>C
AA Mutation	p.Val66Ala(p.V66A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328796
Start	3015928:3015928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94G>T
AA Mutation	p.Val32Leu(p.V32L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328796
Start	3015497:3015497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328796
Start	3015524:3015525(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.497dupT
AA Mutation	p.Leu166PhefsTer48(p.L166Ffs*48)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CLDN6

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328796
Start	3015902:3015902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776424991
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript