Colon Cancer: Gene >> LARS

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394434
Start	146157404:146157404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064A>G
AA Mutation	p.Glu355Gly(p.E355G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146153218:146153218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1240G>A
AA Mutation	p.Ala414Thr(p.A414T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394434
Start	146157626:146157626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.842G>A
AA Mutation	p.Gly281Asp(p.G281D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146177661:146177661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11G>T
AA Mutation	p.Arg4Ile(p.R4I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146168241:146168241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319G>A
AA Mutation	p.Glu107Lys(p.E107K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146157412:146157412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1056A>C
AA Mutation	p.Leu352Phe(p.L352F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146129076:146129076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2671G>A
AA Mutation	p.Val891Ile(p.V891I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146135640:146135640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2173C>T
AA Mutation	p.Leu725Phe(p.L725F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146144309:146144309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1696G>T
AA Mutation	p.Gly566Cys(p.G566C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146171958:146171958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246A>T
AA Mutation	p.Lys82Asn(p.K82N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146126488:146126488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2938C>T
AA Mutation	p.Pro980Ser(p.P980S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146157461:146157461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007A>G
AA Mutation	p.Tyr336Cys(p.Y336C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146128757:146128757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2795A>C
AA Mutation	p.Lys932Thr(p.K932T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146114228:146114228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201386463
CDS Mutation	c.3409G>A
AA Mutation	p.Glu1137Lys(p.E1137K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146130086:146130086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2560G>T
AA Mutation	p.Val854Phe(p.V854F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394434
Start	146149624:146149624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139960441
CDS Mutation	c.1501G>A
AA Mutation	p.Ala501Thr(p.A501T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394434
Start	146114133:146114133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201583773
CDS Mutation	c.3504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394434
Start	146149682:146149682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756908193
CDS Mutation	c.1443A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394434
Start	146172726:146172726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201410450
CDS Mutation	c.174C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394434
Start	146157436:146157436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749791589
CDS Mutation	c.1032C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394434
Start	146171958:146171958(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.246delA
AA Mutation	p.Lys82AsnfsTer23(p.K82Nfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000394434
Start	146129013:146129013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199516658
CDS Mutation	c.2734C>T
AA Mutation	p.Arg912Ter(p.R912*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394434
Start	146130084:146130085(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2561_2562insACTCACTT
AA Mutation	p.Gln855LeufsTer30(p.Q855Lfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000394434
Start	146143509:146143510(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1779_1780insAATATCACAACT
AA Mutation	p.Ser593_Leu594insAsnIleThrThr(p.S593_L594insNITT)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146164402:146164402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767396724
CDS Mutation	c.502G>A
AA Mutation	p.Asp168Asn(p.D168N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146122544:146122544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3140A>C
AA Mutation	p.Lys1047Thr(p.K1047T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394434
Start	146164320:146164320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584T>C
AA Mutation	p.Met195Thr(p.M195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript