Colon Cancer: Gene >> ZNF587B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442832
Start	57840997:57840997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323C>G
AA Mutation	p.Ala108Gly(p.A108G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442832
Start	57841138:57841138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536669289
CDS Mutation	c.464C>T
AA Mutation	p.Ala155Val(p.A155V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000442832
Start	57841795:57841795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754610723
CDS Mutation	c.1121G>A
AA Mutation	p.Arg374His(p.R374H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000442832
Start	57841410:57841410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771557640
CDS Mutation	c.736G>A
AA Mutation	p.Glu246Lys(p.E246K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000442832
Start	57841618:57841618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.944G>A
AA Mutation	p.Arg315His(p.R315H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF587B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442832
Start	57830556:57830556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.28T>C
AA Mutation	p.Ser10Pro(p.S10P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript