Colon Cancer: Gene >> ARHGEF40

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21074650:21074650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920G>A
AA Mutation	p.Gly307Asp(p.G307D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21076617:21076617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1891C>A
AA Mutation	p.Leu631Ile(p.L631I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21082422:21082422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3430G>A
AA Mutation	p.Glu1144Lys(p.E1144K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21074257:21074257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527T>C
AA Mutation	p.Leu176Pro(p.L176P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21082104:21082104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201070551
CDS Mutation	c.3236G>A
AA Mutation	p.Arg1079His(p.R1079H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21074929:21074929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199T>C
AA Mutation	p.Leu400Pro(p.L400P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21075436:21075436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555T>C
AA Mutation	p.Ser519Pro(p.S519P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21074200:21074200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753025691
CDS Mutation	c.470G>A
AA Mutation	p.Arg157Gln(p.R157Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21080699:21080699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2413G>A
AA Mutation	p.Ala805Thr(p.A805T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21085770:21085770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4042G>C
AA Mutation	p.Glu1348Gln(p.E1348Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21084025:21084025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376203053
CDS Mutation	c.3764C>T
AA Mutation	p.Ala1255Val(p.A1255V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21081896:21081896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3028G>T
AA Mutation	p.Ala1010Ser(p.A1010S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298694
Start	21074558:21074558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769665953
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298694
Start	21085829:21085829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4101T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298694
Start	21081877:21081877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3009C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298694
Start	21078227:21078227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2085G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298694
Start	21074666:21074666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764423064
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298694
Start	21082069:21082069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768385826
CDS Mutation	c.3201C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298694
Start	21082320:21082320(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3332delC
AA Mutation	p.Pro1111LeufsTer5(p.P1111Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298694
Start	21088033:21088033(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4459delC
AA Mutation	p.His1487ThrfsTer15(p.H1487Tfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298694
Start	21082089:21082089(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3226delC
AA Mutation	p.Arg1076GlyfsTer18(p.R1076Gfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298694
Start	21078445:21078445(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749402223
CDS Mutation	c.2209delG
AA Mutation	p.Ala737ProfsTer3(p.A737Pfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298694
Start	21078255:21078256(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2113_2114insAGTTT
AA Mutation	p.Ala705GlufsTer26(p.A705Efs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGEF40

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298694
Start	21080676:21080676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2390C>T
AA Mutation	p.Ser797Leu(p.S797L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298694
Start	21074996:21074996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266G>A
Mutation Classification	Silent
Feature Type	Transcript