Colon Cancer: Gene >> GINS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276533
Start	41539967:41539967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.447G>C
AA Mutation	p.Met149Ile(p.M149I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276533
Start	41539924:41539924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775844956
CDS Mutation	c.404C>T
AA Mutation	p.Ala135Val(p.A135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276533
Start	41539697:41539697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317A>G
AA Mutation	p.His106Arg(p.H106R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000276533
Start	41541870:41541870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.546A>G
AA Mutation	p.Ile182Met(p.I182M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276533
Start	41541844:41541844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276533
Start	41537254:41537254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276533
Start	41539952:41539952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762087855
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GINS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276533
Start	41537282:41537282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779030440
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276533
Start	41539734:41539734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.354G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276533
Start	41539925:41539925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747443753
CDS Mutation	c.405G>A
Mutation Classification	Silent
Feature Type	Transcript