Colon Cancer: Gene >> PSMC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000157812
Start	39974619:39974619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565G>A
AA Mutation	p.Glu189Lys(p.E189K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000157812
Start	39974772:39974772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617G>T
AA Mutation	p.Gly206Val(p.G206V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000157812
Start	39974406:39974406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000157812
Start	39974747:39974747(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.598delC
AA Mutation	p.Arg200GlufsTer65(p.R200Efs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PSMC4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000157812
Start	39980336:39980336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.969G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000157812
Start	39974618:39974618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201936053
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript