Colon Cancer: Gene >> ARHGEF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361247
Start	155965335:155965335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.548G>A
AA Mutation	p.Arg183Gln(p.R183Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361247
Start	155950878:155950878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377007664
CDS Mutation	c.2654G>A
AA Mutation	p.Arg885His(p.R885H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361247
Start	155954919:155954919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1766A>T
AA Mutation	p.Tyr589Phe(p.Y589F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361247
Start	155965072:155965072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.640G>A
AA Mutation	p.Ala214Thr(p.A214T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361247
Start	155950464:155950464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2722C>T
AA Mutation	p.Arg908Cys(p.R908C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361247
Start	155951019:155951019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2513G>A
AA Mutation	p.Arg838Gln(p.R838Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361247
Start	155962185:155962185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1139T>C
AA Mutation	p.Val380Ala(p.V380A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361247
Start	155957761:155957761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1667G>A
AA Mutation	p.Arg556Gln(p.R556Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361247
Start	155951497:155951497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2245C>A
AA Mutation	p.Leu749Ile(p.L749I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361247
Start	155951232:155951232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2300T>C
AA Mutation	p.Phe767Ser(p.F767S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361247
Start	155978377:155978377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361247
Start	155957847:155957847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1581C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361247
Start	155952147:155952147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762316330
CDS Mutation	c.2073C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361247
Start	155951258:155951258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2274G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGEF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361247
Start	155952815:155952815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1797G>T
AA Mutation	p.Gln599His(p.Q599H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000361247
Start	155951773:155951773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2176C>T
AA Mutation	p.Arg726Ter(p.R726*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000361247
Start	155952814:155952814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1798A>T
AA Mutation	p.Lys600Ter(p.K600*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript