Colon Cancer: Gene >> ARHGEF17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73309923:73309923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285C>T
AA Mutation	p.Arg429Trp(p.R429W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73310229:73310229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769389453
CDS Mutation	c.1591C>T
AA Mutation	p.Arg531Cys(p.R531C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73309729:73309729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1091A>T
AA Mutation	p.Asp364Val(p.D364V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73310205:73310205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1567C>A
AA Mutation	p.Pro523Thr(p.P523T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73311697:73311697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3059C>T
AA Mutation	p.Pro1020Leu(p.P1020L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73363238:73363238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5029G>A
AA Mutation	p.Ala1677Thr(p.A1677T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73362687:73362687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756636153
CDS Mutation	c.4949C>T
AA Mutation	p.Thr1650Met(p.T1650M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73310073:73310073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201544882
CDS Mutation	c.1435C>T
AA Mutation	p.Arg479Cys(p.R479C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73362165:73362165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4620G>T
AA Mutation	p.Glu1540Asp(p.E1540D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73310173:73310173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1535G>A
AA Mutation	p.Gly512Asp(p.G512D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73356745:73356745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3877A>G
AA Mutation	p.Met1293Val(p.M1293V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73355587:73355587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3508A>G
AA Mutation	p.Asn1170Asp(p.N1170D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73355871:73355871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376468445
CDS Mutation	c.3581G>A
AA Mutation	p.Arg1194His(p.R1194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73311534:73311534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2896T>C
AA Mutation	p.Phe966Leu(p.F966L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73311082:73311082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2444A>G
AA Mutation	p.Asp815Gly(p.D815G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73310725:73310725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2087C>T
AA Mutation	p.Ser696Leu(p.S696L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73357119:73357119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368051277
CDS Mutation	c.3986G>A
AA Mutation	p.Arg1329His(p.R1329H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73310227:73310227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573060878
CDS Mutation	c.1589C>T
AA Mutation	p.Thr530Met(p.T530M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73357118:73357118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3985C>T
AA Mutation	p.Arg1329Cys(p.R1329C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73311484:73311484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775779249
CDS Mutation	c.2846G>A
AA Mutation	p.Arg949Gln(p.R949Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263674
Start	73367672:73367672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747371689
CDS Mutation	c.6084T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263674
Start	73362075:73362075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200742689
CDS Mutation	c.4530G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263674
Start	73310396:73310396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1758C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263674
Start	73357311:73357311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144162252
CDS Mutation	c.4071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263674
Start	73310858:73310858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2220G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263674
Start	73355574:73355574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771650545
CDS Mutation	c.3495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263674
Start	73352916:73352916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764825146
CDS Mutation	c.3357G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263674
Start	73356231:73356231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151080372
CDS Mutation	c.3720G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263674
Start	73311321:73311321(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2687delC
AA Mutation	p.Pro896LeufsTer22(p.P896Lfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263674
Start	73311670:73311670(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3032delT
AA Mutation	p.Met1011SerfsTer2(p.M1011Sfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263674
Start	73309504:73309504(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.869delG
AA Mutation	p.Gly290GlufsTer24(p.G290Efs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263674
Start	73310482:73310482(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1850delC
AA Mutation	p.Pro617LeufsTer10(p.P617Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000263674
Start	73363262:73363262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5053G>T
AA Mutation	p.Glu1685Ter(p.E1685*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGEF17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73311534:73311534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2896T>G
AA Mutation	p.Phe966Val(p.F966V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73356181:73356181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3670C>A
AA Mutation	p.Leu1224Met(p.L1224M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263674
Start	73309569:73309569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931G>A
AA Mutation	p.Asp311Asn(p.D311N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263674
Start	73362117:73362117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4572C>T
Mutation Classification	Silent
Feature Type	Transcript