Colon Cancer: Gene >> CSF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225474
Start	40016297:40016297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.269C>A
AA Mutation	p.Pro90His(p.P90H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225474
Start	40016528:40016528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356A>G
AA Mutation	p.Gln119Arg(p.Q119R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225474
Start	40016505:40016505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225474
Start	40016538:40016538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225474
Start	40015742:40015742(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.97delC
AA Mutation	p.Leu33TrpfsTer16(p.L33Wfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CSF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225474
Start	40016874:40016874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190847104
CDS Mutation	c.539G>A
AA Mutation	p.Arg180Gln(p.R180Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225474
Start	40015797:40015797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147G>A
Mutation Classification	Silent
Feature Type	Transcript