Colon Cancer: Gene >> ARFGAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370283
Start	63276106:63276106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.76G>T
AA Mutation	p.Gly26Cys(p.G26C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370283
Start	63278912:63278912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763879486
CDS Mutation	c.544C>T
AA Mutation	p.Arg182Cys(p.R182C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370283
Start	63284899:63284899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147317838
CDS Mutation	c.751G>A
AA Mutation	p.Val251Ile(p.V251I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370283
Start	63276574:63276574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265T>A
AA Mutation	p.Ser89Thr(p.S89T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370283
Start	63278135:63278135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370283
Start	63282842:63282842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777510216
CDS Mutation	c.708G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370283
Start	63276138:63276138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370283
Start	63287735:63287735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767913835
CDS Mutation	c.1083G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370283
Start	63286407:63286408(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.883dupT
AA Mutation	p.Ser295PhefsTer42(p.S295Ffs*42)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARFGAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370283
Start	63276515:63276515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206A>C
AA Mutation	p.Asp69Ala(p.D69A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370283
Start	63287662:63287662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010C>T
AA Mutation	p.Pro337Leu(p.P337L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript