Colon Cancer: Gene >> GKN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377938
Start	68980765:68980765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200701146
CDS Mutation	c.542C>T
AA Mutation	p.Thr181Met(p.T181M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377938
Start	68977658:68977658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130A>G
AA Mutation	p.Asn44Asp(p.N44D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377938
Start	68979993:68979993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377938
Start	68979999:68979999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202096982
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377938
Start	68980740:68980740(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759880395
CDS Mutation	c.523delT
AA Mutation	p.Tyr175ThrfsTer38(p.Y175Tfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GKN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377938
Start	68974666:68974666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141746794
CDS Mutation	c.31C>T
AA Mutation	p.Arg11Cys(p.R11C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript