Colon Cancer: Gene >> GATA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269216
Start	22182777:22182777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1449G>A
AA Mutation	p.Met483Ile(p.M483I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269216
Start	22181462:22181462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144512170
CDS Mutation	c.1312C>T
AA Mutation	p.Arg438Trp(p.R438W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269216
Start	22171533:22171533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389C>G
AA Mutation	p.Ser130Cys(p.S130C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269216
Start	22182778:22182779(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1454_1455delAA
AA Mutation	p.Lys485ArgfsTer11(p.K485Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000269216
Start	22182830:22182830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1502C>A
AA Mutation	p.Ser501Ter(p.S501*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269216
Start	22182830:22182831(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1505dupA
AA Mutation	p.Thr503AspfsTer5(p.T503Dfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GATA6

No Mutation Annotation!