Colon Cancer: Gene >> MAU2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262815
Start	19355350:19355350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1726C>T
AA Mutation	p.His576Tyr(p.H576Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262815
Start	19321111:19321111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.252G>T
AA Mutation	p.Gln84His(p.Q84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262815
Start	19354391:19354391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1585G>A
AA Mutation	p.Ala529Thr(p.A529T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262815
Start	19349216:19349216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753815220
CDS Mutation	c.1420C>T
AA Mutation	p.Arg474Cys(p.R474C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262815
Start	19345326:19345326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1178A>G
AA Mutation	p.Asn393Ser(p.N393S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262815
Start	19349176:19349176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761860553
CDS Mutation	c.1380C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262815
Start	19354429:19354429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372700362
CDS Mutation	c.1623G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262815
Start	19337193:19337193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776126180
CDS Mutation	c.384G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000262815
Start	19354418:19354418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1612C>T
AA Mutation	p.Gln538Ter(p.Q538*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000262815
Start	19335737:19335737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MAU2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262815
Start	19354368:19354368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1562T>C
AA Mutation	p.Met521Thr(p.M521T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript