Colon Cancer: Gene >> CLN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360019
Start	28486599:28486599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512C>T
AA Mutation	p.Ser171Phe(p.S171F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360019
Start	28487473:28487473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746644433
CDS Mutation	c.443T>G
AA Mutation	p.Val148Gly(p.V148G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360019
Start	28477604:28477604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369801432
CDS Mutation	c.1229C>T
AA Mutation	p.Ala410Val(p.A410V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360019
Start	28486363:28486363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748636727
CDS Mutation	c.661G>A
AA Mutation	p.Ala221Thr(p.A221T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360019
Start	28491746:28491746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14C>T
AA Mutation	p.Ala5Val(p.A5V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360019
Start	28484013:28484013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752632879
CDS Mutation	c.783G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CLN3

No Mutation Annotation!