Colon Cancer: Gene >> CPSF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292476
Start	99448183:99448183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217C>T
AA Mutation	p.Arg73Cys(p.R73C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292476
Start	99448236:99448236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.270G>T
AA Mutation	p.Met90Ile(p.M90I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292476
Start	99453994:99453994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576966048
CDS Mutation	c.599C>T
AA Mutation	p.Ser200Leu(p.S200L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292476
Start	99444796:99444796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769057045
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292476
Start	99454040:99454040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292476
Start	99456440:99456440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292476
Start	99456452:99456452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755817381
CDS Mutation	c.762C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292476
Start	99450313:99450313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.345C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292476
Start	99456437:99456437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767929343
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CPSF4

No Mutation Annotation!