Colon Cancer: Gene >> PSMD6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295901
Start	64019000:64019000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748146502
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Cys(p.R179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295901
Start	64018829:64018829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.706C>T
AA Mutation	p.Leu236Phe(p.L236F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295901
Start	64018999:64018999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536G>A
AA Mutation	p.Arg179His(p.R179H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295901
Start	64018961:64018961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574C>T
AA Mutation	p.Arg192Cys(p.R192C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295901
Start	64022375:64022375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295901
Start	64018624:64018624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000295901
Start	64010746:64010746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1092G>A
AA Mutation	p.Trp364Ter(p.W364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000295901
Start	64010957:64010957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.996-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PSMD6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295901
Start	64022368:64022368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.301C>T
AA Mutation	p.Arg101Cys(p.R101C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript