Colon Cancer: Gene >> ARHGAP17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289968
Start	24952349:24952349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749902519
CDS Mutation	c.986G>A
AA Mutation	p.Arg329Gln(p.R329Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000289968
Start	24979003:24979003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.56C>A
AA Mutation	p.Ala19Asp(p.A19D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000289968
Start	24977317:24977317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750139572
CDS Mutation	c.96T>G
AA Mutation	p.Ile32Met(p.I32M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000289968
Start	24949455:24949455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1076A>G
AA Mutation	p.Asp359Gly(p.D359G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000289968
Start	24935620:24935620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744C>A
AA Mutation	p.Pro582Thr(p.P582T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000289968
Start	24930859:24930859(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2440delC
AA Mutation	p.Gln814AsnfsTer23(p.Q814Nfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000289968
Start	24939460:24939460(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1628delC
AA Mutation	p.Pro543LeufsTer55(p.P543Lfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000289968
Start	24979006:24979006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.54-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289968
Start	24939541:24939541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1547G>T
AA Mutation	p.Arg516Ile(p.R516I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript