Colon Cancer: Gene >> CR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207475189:207475189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2512C>T
AA Mutation	p.Pro838Ser(p.P838S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207473071:207473071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1870G>T
AA Mutation	p.Asp624Tyr(p.D624Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207466672:207466672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205G>T
AA Mutation	p.Asp69Tyr(p.D69Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207470064:207470064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1187A>G
AA Mutation	p.Gln396Arg(p.Q396R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207480004:207480004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2962A>G
AA Mutation	p.Thr988Ala(p.T988A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207477966:207477966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2807T>G
AA Mutation	p.Val936Gly(p.V936G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367058
Start	207468802:207468802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637G>A
AA Mutation	p.Ala213Thr(p.A213T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207475135:207475135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2458T>C
AA Mutation	p.Phe820Leu(p.F820L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207472993:207472993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1792C>A
AA Mutation	p.Leu598Ile(p.L598I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207466831:207466831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364T>C
AA Mutation	p.Phe122Leu(p.F122L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207468805:207468805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201760344
CDS Mutation	c.640C>T
AA Mutation	p.Arg214Cys(p.R214C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207476338:207476338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2644C>A
AA Mutation	p.Gln882Lys(p.Q882K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207466649:207466649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779099901
CDS Mutation	c.182A>C
AA Mutation	p.Lys61Thr(p.K61T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207468824:207468824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147633291
CDS Mutation	c.659G>A
AA Mutation	p.Arg220Gln(p.R220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207471003:207471003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545091003
CDS Mutation	c.1409C>T
AA Mutation	p.Ala470Val(p.A470V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207476300:207476300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756989345
CDS Mutation	c.2606G>A
AA Mutation	p.Arg869Gln(p.R869Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367058
Start	207469921:207469921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144982406
CDS Mutation	c.1044G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367058
Start	207471004:207471004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565317532
CDS Mutation	c.1410G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367058
Start	207466842:207466842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138096192
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367058
Start	207478030:207478030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145934194
CDS Mutation	c.2871G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367058
Start	207472896:207472896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1695A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000367058
Start	207475018:207475018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766671758
CDS Mutation	c.2341C>T
AA Mutation	p.Arg781Ter(p.R781*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367058
Start	207472913:207472914(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1712_1713insTAACAGGG
AA Mutation	p.Glu571AspfsTer59(p.E571Dfs*59)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367058
Start	207476265:207476266(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2571_2572insAGCAACA
AA Mutation	p.Pro858SerfsTer4(p.P858Sfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207466733:207466733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266C>T
AA Mutation	p.Ser89Phe(p.S89F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207469994:207469994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202077872
CDS Mutation	c.1117G>A
AA Mutation	p.Asp373Asn(p.D373N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207475079:207475079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2402A>C
AA Mutation	p.Lys801Thr(p.K801T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207466733:207466733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266C>A
AA Mutation	p.Ser89Tyr(p.S89Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367058
Start	207470819:207470819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305A>G
AA Mutation	p.Ile435Met(p.I435M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000367058
Start	207470739:207470739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1226-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript