Colon Cancer: Gene >> ARHGEF7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111244284:111244284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003G>A
AA Mutation	p.Glu335Lys(p.E335K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111115688:111115688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.162G>T
AA Mutation	p.Glu54Asp(p.E54D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111292150:111292150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2230G>A
AA Mutation	p.Val744Ile(p.V744I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111217776:111217776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629T>C
AA Mutation	p.Val210Ala(p.V210A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111159052:111159052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.278C>A
AA Mutation	p.Pro93His(p.P93H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000218789
Start	111303034:111303034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2039C>T
AA Mutation	p.Ala680Val(p.A680V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111283316:111283316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1966C>T
AA Mutation	p.Arg656Trp(p.R656W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111292193:111292193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2273G>A
AA Mutation	p.Arg758His(p.R758H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111274758:111274758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1303C>A
AA Mutation	p.Gln435Lys(p.Q435K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111273903:111273903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778093839
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409His(p.R409H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111280628:111280628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764936081
CDS Mutation	c.1739C>T
AA Mutation	p.Thr580Met(p.T580M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375741
Start	111292224:111292224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2304A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375741
Start	111275609:111275609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771908591
CDS Mutation	c.1413C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375741
Start	111280298:111280298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1596A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGEF7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111292286:111292286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2366C>T
AA Mutation	p.Ser789Phe(p.S789F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111273889:111273889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1212C>G
AA Mutation	p.Ser404Arg(p.S404R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375741
Start	111244242:111244242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961G>A
AA Mutation	p.Glu321Lys(p.E321K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375741
Start	111273905:111273905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228C>T
Mutation Classification	Silent
Feature Type	Transcript