Colon Cancer: Gene >> ARHGEF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	131043569:131043569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1585A>G
AA Mutation	p.Ile529Val(p.I529V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	130931107:130931107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150G>T
AA Mutation	p.Glu50Asp(p.E50D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	131043540:131043540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536731766
CDS Mutation	c.1556G>A
AA Mutation	p.Arg519Gln(p.R519Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	131040157:131040157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.889C>T
AA Mutation	p.Arg297Trp(p.R297W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	131040052:131040052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>A
AA Mutation	p.Ala262Thr(p.A262T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	131038862:131038862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.577G>A
AA Mutation	p.Asp193Asn(p.D193N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	131041332:131041332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1207G>A
AA Mutation	p.Glu403Lys(p.E403K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	130946543:130946543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335C>A
AA Mutation	p.Ser112Tyr(p.S112Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	131040139:131040139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.871G>A
AA Mutation	p.Glu291Lys(p.E291K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326016
Start	131041448:131041448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326016
Start	131041367:131041367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326016
Start	131038993:131038993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372440562
CDS Mutation	c.708C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326016
Start	131044422:131044422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1723C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326016
Start	131041857:131041857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201353514
CDS Mutation	c.1380C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326016
Start	131040072:131040072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.804C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326016
Start	131040084:131040084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779052727
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326016
Start	131041277:131041277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326016
Start	131038879:131038879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146135621
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGEF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	131041822:131041822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1345A>G
AA Mutation	p.Lys449Glu(p.K449E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	131040306:131040306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.970G>A
AA Mutation	p.Glu324Lys(p.E324K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326016
Start	130931184:130931184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.227G>T
AA Mutation	p.Arg76Ile(p.R76I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326016
Start	131041331:131041331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326016
Start	131040398:131040398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1062G>A
Mutation Classification	Silent
Feature Type	Transcript