Colon Cancer: Gene >> GATA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335135
Start	11749000:11749000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.698C>T
AA Mutation	p.Thr233Met(p.T233M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335135
Start	11757034:11757034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781198110
CDS Mutation	c.1097C>T
AA Mutation	p.Thr366Met(p.T366M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335135
Start	11750195:11750195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868C>T
AA Mutation	p.Pro290Ser(p.P290S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335135
Start	11750121:11750121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745533633
CDS Mutation	c.794G>A
AA Mutation	p.Arg265His(p.R265H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335135
Start	11756969:11756969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755482369
CDS Mutation	c.1032C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335135
Start	11758439:11758439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1293C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GATA4

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335135
Start	11758362:11758363(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1220dupC
AA Mutation	p.Gln408ThrfsTer54(p.Q408Tfs*54)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript