Colon Cancer: Gene >> INSRR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156849401:156849401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1289C>T
AA Mutation	p.Ala430Val(p.A430V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156845660:156845660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2133G>T
AA Mutation	p.Lys711Asn(p.K711N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156841016:156841016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759533268
CDS Mutation	c.3751C>T
AA Mutation	p.Arg1251Trp(p.R1251W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156845157:156845157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2356G>A
AA Mutation	p.Asp786Asn(p.D786N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156854066:156854066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374655019
CDS Mutation	c.323G>A
AA Mutation	p.Arg108His(p.R108H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156841705:156841705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3487T>C
AA Mutation	p.Ser1163Pro(p.S1163P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156854165:156854165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139920561
CDS Mutation	c.224G>A
AA Mutation	p.Arg75His(p.R75H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156853869:156853869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200875065
CDS Mutation	c.520G>A
AA Mutation	p.Glu174Lys(p.E174K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156851724:156851724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006G>A
AA Mutation	p.Asp336Asn(p.D336N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156844778:156844778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2503C>T
AA Mutation	p.Arg835Cys(p.R835C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156844542:156844542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2657A>G
AA Mutation	p.Tyr886Cys(p.Y886C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156849030:156849030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1462C>T
AA Mutation	p.Arg488Cys(p.R488C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156851930:156851930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899G>T
AA Mutation	p.Cys300Phe(p.C300F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156844818:156844818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2463G>T
AA Mutation	p.Lys821Asn(p.K821N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156851743:156851743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987G>T
AA Mutation	p.Lys329Asn(p.K329N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156849438:156849438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1252G>A
AA Mutation	p.Asp418Asn(p.D418N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156844271:156844271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2747A>G
AA Mutation	p.Asp916Gly(p.D916G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156845684:156845684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2109G>T
AA Mutation	p.Glu703Asp(p.E703D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156846593:156846593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377121387
CDS Mutation	c.1736C>T
AA Mutation	p.Thr579Met(p.T579M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156841072:156841072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3695A>G
AA Mutation	p.Asn1232Ser(p.N1232S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156845135:156845135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2378C>T
AA Mutation	p.Ala793Val(p.A793V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368195
Start	156846616:156846616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201065454
CDS Mutation	c.1713C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368195
Start	156854104:156854104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143166774
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368195
Start	156852145:156852145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.684C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368195
Start	156842206:156842206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746766711
CDS Mutation	c.3303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368195
Start	156846664:156846668(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1661_1665delGCACC
AA Mutation	p.Arg554ProfsTer28(p.R554Pfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368195
Start	156844551:156844551(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2648delC
AA Mutation	p.Pro883LeufsTer74(p.P883Lfs*74)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368195
Start	156851382:156851383(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1136_1137delCT
AA Mutation	p.Thr379ArgfsTer91(p.T379Rfs*91)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368195
Start	156844261:156844261(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs772259106
CDS Mutation	c.2757delG
AA Mutation	p.Leu920CysfsTer37(p.L920Cfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000368195
Start	156851420:156851420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184000730
CDS Mutation	c.1099C>T
AA Mutation	p.Gln367Ter(p.Q367*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000368195
Start	156844174:156844174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2843+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> INSRR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156852017:156852017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812C>A
AA Mutation	p.Ser271Tyr(p.S271Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368195
Start	156853970:156853970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748927042
CDS Mutation	c.419G>A
AA Mutation	p.Arg140His(p.R140H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368195
Start	156845249:156845249(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2264delG
AA Mutation	p.Gly755AlafsTer20(p.G755Afs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000368195
Start	156846534:156846534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552398222
CDS Mutation	c.1795C>T
AA Mutation	p.Arg599Ter(p.R599*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript