Colon Cancer: Gene >> CLDN9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000445369
Start	3013478:3013478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.116G>T
AA Mutation	p.Ser39Ile(p.S39I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000445369
Start	3013472:3013472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746271447
CDS Mutation	c.110G>A
AA Mutation	p.Gly37Asp(p.G37D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000445369
Start	3013448:3013448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.86T>C
AA Mutation	p.Leu29Pro(p.L29P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445369
Start	3013749:3013749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145578676
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000445369
Start	3013894:3013894(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.537delG
AA Mutation	p.Leu180SerfsTer196(p.L180Sfs*196)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CLDN9

No Mutation Annotation!