Colon Cancer: Gene >> ERCC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127286967:127286967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754010782
CDS Mutation	c.1078C>T
AA Mutation	p.Arg360Cys(p.R360C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127271381:127271381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1900C>T
AA Mutation	p.Arg634Cys(p.R634C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127289817:127289817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139690693
CDS Mutation	c.529G>A
AA Mutation	p.Val177Ile(p.V177I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127280505:127280505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1469A>G
AA Mutation	p.Glu490Gly(p.E490G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127286862:127286862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183G>A
AA Mutation	p.Asp395Asn(p.D395N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127288851:127288851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836A>C
AA Mutation	p.Glu279Ala(p.E279A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127259330:127259330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2183T>A
AA Mutation	p.Val728Glu(p.V728E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127288829:127288829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858C>A
AA Mutation	p.His286Gln(p.H286Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127293649:127293649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98A>G
AA Mutation	p.Asp33Gly(p.D33G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127257717:127257717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770995913
CDS Mutation	c.2228G>A
AA Mutation	p.Arg743His(p.R743H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285398
Start	127272949:127272949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147061557
CDS Mutation	c.1743C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285398
Start	127286824:127286824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1221T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285398
Start	127259440:127259440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540496066
CDS Mutation	c.2073G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285398
Start	127286785:127286785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1260C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ERCC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127286789:127286789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1256G>T
AA Mutation	p.Arg419Met(p.R419M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127280530:127280530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1444T>C
AA Mutation	p.Phe482Leu(p.F482L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript