Colon Cancer: Gene >> PPM1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282412
Start	44201567:44201567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368T>C
AA Mutation	p.Leu123Pro(p.L123P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282412
Start	44201552:44201552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758211363
CDS Mutation	c.353G>A
AA Mutation	p.Arg118His(p.R118H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282412
Start	44218036:44218036(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1037delA
AA Mutation	p.Asn346IlefsTer25(p.N346Ifs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000282412
Start	44201766:44201768(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.569_571delAAC
AA Mutation	p.Gln190del(p.Q190del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PPM1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282412
Start	44201797:44201797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201987533
CDS Mutation	c.598C>T
AA Mutation	p.Arg200Cys(p.R200C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282412
Start	44201770:44201770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571C>T
AA Mutation	p.Arg191Cys(p.R191C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282412
Start	44217986:44217986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150223863
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript