Colon Cancer: Gene >> ADGRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000567835
Start	57659457:57659457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1349T>C
AA Mutation	p.Leu450Pro(p.L450P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000567835
Start	57657380:57657380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770060105
CDS Mutation	c.1175C>T
AA Mutation	p.Ser392Leu(p.S392L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000567835
Start	57653315:57653315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000567835
Start	57655899:57655899(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.926delG
AA Mutation	p.Gly309ValfsTer14(p.G309Vfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000567835
Start	57656241:57656241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033C>T
AA Mutation	p.Gln345Ter(p.Q345*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ADGRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000567835
Start	57655881:57655881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906G>T
AA Mutation	p.Lys302Asn(p.K302N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript