Colon Cancer: Gene >> ARHGAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311956
Start	46680653:46680653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>T
AA Mutation	p.Val244Phe(p.V244F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311956
Start	46679413:46679413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773769674
CDS Mutation	c.1083C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311956
Start	46680681:46680681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779455505
CDS Mutation	c.702G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311956
Start	46695710:46695711(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.178_179delTG
AA Mutation	p.Trp60GlyfsTer2(p.W60Gfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311956
Start	46680674:46680674(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.709delC
AA Mutation	p.Leu237CysfsTer135(p.L237Cfs*135)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311956
Start	46680673:46680673(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs754492553
CDS Mutation	c.710delT
AA Mutation	p.Leu237ArgfsTer135(p.L237Rfs*135)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311956
Start	46695684:46695684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760960194
CDS Mutation	c.205C>T
AA Mutation	p.Arg69Trp(p.R69W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript