Colon Cancer: Gene >> ARHGAP9

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000393791
Start	57474877:57474877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1649G>T
AA Mutation	p.Arg550Ile(p.R550I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000393791
Start	57475396:57475396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1447C>T
AA Mutation	p.Arg483Trp(p.R483W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393791
Start	57473647:57473647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1980G>T
AA Mutation	p.Lys660Asn(p.K660N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393791
Start	57479168:57479168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239C>T
AA Mutation	p.Ala80Val(p.A80V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393791
Start	57476942:57476942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749408492
CDS Mutation	c.892C>T
AA Mutation	p.Arg298Cys(p.R298C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393791
Start	57475570:57475570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1357G>A
AA Mutation	p.Ala453Thr(p.A453T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000393791
Start	57478581:57478581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493C>A
AA Mutation	p.Leu165Ile(p.L165I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000393791
Start	57479211:57479211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367755619
CDS Mutation	c.196C>T
AA Mutation	p.Arg66Cys(p.R66C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000393791
Start	57479121:57479121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761890422
CDS Mutation	c.286G>A
AA Mutation	p.Val96Ile(p.V96I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393791
Start	57478591:57478591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145600928
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393791
Start	57476892:57476892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.942G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393791
Start	57473614:57473614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2013G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393791
Start	57476406:57476406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393791
Start	57479113:57479113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199948954
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393791
Start	57475337:57475337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1506G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393791
Start	57472561:57472561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393791
Start	57472592:57472592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2121C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000393791
Start	57477554:57477554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661C>T
AA Mutation	p.Gln221Ter(p.Q221*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000393791
Start	57476963:57476964(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.871-1_871insAAATGGGA
AA Mutation	p.Gly291LysfsTer44(p.G291Kfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393791
Start	57472650:57472651(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2062dupC
AA Mutation	p.His688ProfsTer20(p.H688Pfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393791
Start	57475909:57475909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1235A>C
AA Mutation	p.Glu412Ala(p.E412A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393791
Start	57477481:57477481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144828330
CDS Mutation	c.734C>T
AA Mutation	p.Pro245Leu(p.P245L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393791
Start	57479381:57479381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26G>A
AA Mutation	p.Ser9Asn(p.S9N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393791
Start	57473675:57473676(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1951_1952insAC
AA Mutation	p.Ile651AsnfsTer5(p.I651Nfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript