Colon Cancer: Gene >> SMC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110596415:110596415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1981C>T
AA Mutation	p.Arg661Trp(p.R661W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110599772:110599772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2387G>T
AA Mutation	p.Arg796Ile(p.R796I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110593176:110593176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1916C>T
AA Mutation	p.Ser639Leu(p.S639L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110584209:110584209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377731006
CDS Mutation	c.1118C>T
AA Mutation	p.Thr373Met(p.T373M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361804
Start	110577837:110577837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273C>G
AA Mutation	p.Ile91Met(p.I91M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110596413:110596413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1979A>G
AA Mutation	p.His660Arg(p.H660R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110602884:110602884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3357G>T
AA Mutation	p.Gln1119His(p.Q1119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110584349:110584349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258T>G
AA Mutation	p.Leu420Val(p.L420V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110589705:110589705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1406G>T
AA Mutation	p.Arg469Ile(p.R469I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110601973:110601973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761995373
CDS Mutation	c.2900G>A
AA Mutation	p.Arg967Gln(p.R967Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110602565:110602565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3197A>C
AA Mutation	p.Gln1066Pro(p.Q1066P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361804
Start	110591030:110591030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1710G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361804
Start	110601809:110601809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2817T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SMC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110584214:110584214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123C>A
AA Mutation	p.Leu375Ile(p.L375I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361804
Start	110596548:110596548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2114A>G
AA Mutation	p.Glu705Gly(p.E705G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110590544:110590544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1642A>G
AA Mutation	p.Thr548Ala(p.T548A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361804
Start	110602646:110602646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3278T>G
AA Mutation	p.Phe1093Cys(p.F1093C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361804
Start	110602629:110602629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556688502
CDS Mutation	c.3261C>T
Mutation Classification	Silent
Feature Type	Transcript