Colon Cancer: Gene >> ARHGEF15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8313054:8313054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766415435
CDS Mutation	c.734G>A
AA Mutation	p.Arg245Gln(p.R245Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8319326:8319326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775473270
CDS Mutation	c.2201G>A
AA Mutation	p.Arg734His(p.R734H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8318397:8318397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771433483
CDS Mutation	c.1715G>A
AA Mutation	p.Arg572His(p.R572H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8318600:8318600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587777166
CDS Mutation	c.1810C>T
AA Mutation	p.Arg604Cys(p.R604C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8318774:8318774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193921031
CDS Mutation	c.1897C>T
AA Mutation	p.Arg633Trp(p.R633W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8312073:8312073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34C>T
AA Mutation	p.Pro12Ser(p.P12S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8312292:8312292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253C>A
AA Mutation	p.Leu85Ile(p.L85I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8315173:8315173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1156C>A
AA Mutation	p.Pro386Thr(p.P386T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8312454:8312454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200188980
CDS Mutation	c.415G>A
AA Mutation	p.Ala139Thr(p.A139T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8312193:8312193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.154G>T
AA Mutation	p.Asp52Tyr(p.D52Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8318601:8318601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143720339
CDS Mutation	c.1811G>A
AA Mutation	p.Arg604His(p.R604H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8320926:8320926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2459G>A
AA Mutation	p.Arg820His(p.R820H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361926
Start	8318570:8318570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1780A>G
AA Mutation	p.Ile594Val(p.I594V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361926
Start	8313120:8313120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800G>A
AA Mutation	p.Arg267His(p.R267H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361926
Start	8312150:8312150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361926
Start	8316043:8316043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1599C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361926
Start	8318643:8318643(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1853delT
AA Mutation	p.Leu618ArgfsTer24(p.L618Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361926
Start	8312070:8312070(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.36delC
AA Mutation	p.Thr13ArgfsTer169(p.T13Rfs*169)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361926
Start	8313205:8313205(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.890delC
AA Mutation	p.Pro297HisfsTer39(p.P297Hfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361926
Start	8318819:8318820(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs752138065
CDS Mutation	c.1949dupG
AA Mutation	p.Val651ArgfsTer18(p.V651Rfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	start_lost
Transcription ID	ENST00000361926
Start	8312041:8312041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2T>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGEF15

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361926
Start	8316021:8316021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1577A>G
AA Mutation	p.Asp526Gly(p.D526G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361926
Start	8315265:8315265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1248G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000361926
Start	8319311:8319311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2187-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript