Colon Cancer: Gene >> LIN28A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254231
Start	26425371:26425371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.297G>C
AA Mutation	p.Lys99Asn(p.K99N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254231
Start	26411502:26411502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148C>T
AA Mutation	p.Arg50Cys(p.R50C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254231
Start	26411513:26411513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760812729
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254231
Start	26411540:26411540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000254231
Start	26426397:26426398(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.569_570insGTACAAAG
AA Mutation	p.Tyr190Ter(p.Y190*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LIN28A

No Mutation Annotation!