Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DUOX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45142019:45142019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1729C>T
AA Mutation	p.Pro577Ser(p.P577S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45155871:45155871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142004175
CDS Mutation	c.3644G>A
AA Mutation	p.Arg1215His(p.R1215H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45135286:45135286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490G>T
AA Mutation	p.Asp164Tyr(p.D164Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45141050:45141050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1545G>T
AA Mutation	p.Trp515Cys(p.W515C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45135249:45135249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453G>T
AA Mutation	p.Trp151Cys(p.W151C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45143288:45143288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139397185
CDS Mutation	c.1921G>A
AA Mutation	p.Val641Met(p.V641M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45161914:45161914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4033C>A
AA Mutation	p.Arg1345Ser(p.R1345S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45135535:45135535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557G>A
AA Mutation	p.Ser186Asn(p.S186N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45161753:45161753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3872G>T
AA Mutation	p.Arg1291Leu(p.R1291L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45152507:45152507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76605732
CDS Mutation	c.3415G>A
AA Mutation	p.Val1139Ile(p.V1139I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45151188:45151188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2954G>C
AA Mutation	p.Arg985Thr(p.R985T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45144929:45144929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763581105
CDS Mutation	c.2171C>T
AA Mutation	p.Ala724Val(p.A724V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45153439:45153439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151144648
CDS Mutation	c.3484G>A
AA Mutation	p.Val1162Ile(p.V1162I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45134262:45134262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260C>T
AA Mutation	p.Ala87Val(p.A87V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45134259:45134259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.257C>A
AA Mutation	p.Pro86His(p.P86H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45152300:45152300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3208G>A
AA Mutation	p.Ala1070Thr(p.A1070T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45164782:45164782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756591126
CDS Mutation	c.4537C>T
AA Mutation	p.Arg1513Trp(p.R1513W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45161900:45161900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4019G>T
AA Mutation	p.Gly1340Val(p.G1340V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45144105:45144105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150755159
CDS Mutation	c.2006G>A
AA Mutation	p.Arg669His(p.R669H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000321429
Start	45152050:45152050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3191A>G
AA Mutation	p.Tyr1064Cys(p.Y1064C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45142044:45142044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370040367
CDS Mutation	c.1754G>A
AA Mutation	p.Arg585His(p.R585H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45136606:45136606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003C>T
AA Mutation	p.Pro335Ser(p.P335S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45152293:45152293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3201C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45164790:45164790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367674334
CDS Mutation	c.4545C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45135285:45135285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45135261:45135261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.465C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45161874:45161874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139578501
CDS Mutation	c.3993G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45142087:45142087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140249290
CDS Mutation	c.1797C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45139533:45139533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1323A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45143275:45143275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765157482
CDS Mutation	c.1908G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45136569:45136569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45144206:45144206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45151159:45151159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752609301
CDS Mutation	c.2925C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45162335:45162335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4206G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DUOX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45164884:45164884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4639C>T
AA Mutation	p.His1547Tyr(p.H1547Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45164820:45164820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4575G>A
AA Mutation	p.Met1525Ile(p.M1525I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45164791:45164791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747262030
CDS Mutation	c.4546G>A
AA Mutation	p.Gly1516Arg(p.G1516R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45163540:45163540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4257C>A
AA Mutation	p.Phe1419Leu(p.F1419L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321429
Start	45148384:45148384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2755G>A
AA Mutation	p.Asp919Asn(p.D919N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45144151:45144151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2052G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321429
Start	45162308:45162308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768386196
CDS Mutation	c.4179C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant
Transcription ID	ENST00000321429
Start	45155801:45155810(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3576_3585delCCTCACGGGG
AA Mutation	p.Thr1194CysfsTer4(p.X1192_splice)
Mutation Classification	Splice_Site
Feature Type	Transcript