Colon Cancer: Gene >> IQGAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156537275:156537275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143078859
CDS Mutation	c.3328G>A
AA Mutation	p.Glu1110Lys(p.E1110K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156561869:156561869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010A>G
AA Mutation	p.Gln337Arg(p.Q337R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156544207:156544207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560536788
CDS Mutation	c.2405G>A
AA Mutation	p.Arg802Gln(p.R802Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156540790:156540790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367772740
CDS Mutation	c.2657G>A
AA Mutation	p.Arg886Gln(p.R886Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156530196:156530196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781305314
CDS Mutation	c.4313G>A
AA Mutation	p.Arg1438Gln(p.R1438Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156537262:156537262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138382649
CDS Mutation	c.3341G>A
AA Mutation	p.Arg1114Gln(p.R1114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156548641:156548641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11264496
CDS Mutation	c.1933G>A
AA Mutation	p.Asp645Asn(p.D645N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156554385:156554385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1298G>A
AA Mutation	p.Gly433Asp(p.G433D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156561975:156561975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.904G>A
AA Mutation	p.Asp302Asn(p.D302N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156548152:156548152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371514554
CDS Mutation	c.2225G>A
AA Mutation	p.Arg742His(p.R742H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156563150:156563150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.782C>T
AA Mutation	p.Ala261Val(p.A261V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156538992:156538992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3098C>A
AA Mutation	p.Pro1033Gln(p.P1033Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156554269:156554269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414G>T
AA Mutation	p.Gly472Cys(p.G472C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156564642:156564642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749747273
CDS Mutation	c.410G>A
AA Mutation	p.Arg137Gln(p.R137Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156529076:156529076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748938834
CDS Mutation	c.4411C>T
AA Mutation	p.Arg1471Cys(p.R1471C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156544004:156544004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2507C>T
AA Mutation	p.Ala836Val(p.A836V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361170
Start	156563135:156563135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797A>G
AA Mutation	p.His266Arg(p.H266R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156563630:156563630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.542A>G
AA Mutation	p.Lys181Arg(p.K181R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361170
Start	156528033:156528033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778757420
CDS Mutation	c.4701G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361170
Start	156537297:156537297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763913370
CDS Mutation	c.3306G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361170
Start	156550310:156550310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1776C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361170
Start	156535187:156535187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776558515
CDS Mutation	c.3483C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361170
Start	156534628:156534628(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3613delC
AA Mutation	p.Gln1205SerfsTer31(p.Q1205Sfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000361170
Start	156530305:156530305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4204A>T
AA Mutation	p.Lys1402Ter(p.K1402*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000361170
Start	156533772:156533772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3976+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000361170
Start	156551973:156551973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139298563
CDS Mutation	c.1570+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> IQGAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156530145:156530145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4364C>T
AA Mutation	p.Ala1455Val(p.A1455V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361170
Start	156540884:156540884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751001051
CDS Mutation	c.2563C>T
AA Mutation	p.Arg855Cys(p.R855C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361170
Start	156533786:156533786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3963C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361170
Start	156552089:156552089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377601754
CDS Mutation	c.1455C>T
Mutation Classification	Silent
Feature Type	Transcript