Colon Cancer: Gene >> MUM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1360463:1360463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545G>A
AA Mutation	p.Arg182Lys(p.R182K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1367213:1367213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145648400
CDS Mutation	c.1418C>T
AA Mutation	p.Thr473Met(p.T473M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1369316:1369316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1477A>T
AA Mutation	p.Ile493Phe(p.I493F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1360943:1360943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1025G>C
AA Mutation	p.Ser342Thr(p.S342T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1369640:1369640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1546G>T
AA Mutation	p.Asp516Tyr(p.D516Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1360184:1360184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266G>C
AA Mutation	p.Arg89Thr(p.R89T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1370680:1370680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1591G>T
AA Mutation	p.Gly531Trp(p.G531W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1360270:1360270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189340337
CDS Mutation	c.352C>T
AA Mutation	p.Arg118Trp(p.R118W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1370780:1370780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1691G>T
AA Mutation	p.Arg564Leu(p.R564L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1370731:1370731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1642G>T
AA Mutation	p.Gly548Trp(p.G548W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000591806
Start	1369294:1369294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780510623
CDS Mutation	c.1455C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000591806
Start	1364529:1364529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237G>T
AA Mutation	p.Gly413Ter(p.G413*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MUM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1366331:1366331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1314G>T
AA Mutation	p.Lys438Asn(p.K438N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000591806
Start	1362291:1362291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750747499
CDS Mutation	c.1156C>T
AA Mutation	p.Arg386Cys(p.R386C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript