Colon Cancer: Gene >> PFDN4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371419
Start	54214400:54214400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.74A>C
AA Mutation	p.Lys25Thr(p.K25T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371419
Start	54215415:54215415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.248C>T
AA Mutation	p.Thr83Met(p.T83M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371419
Start	54214378:54214378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52G>A
AA Mutation	p.Glu18Lys(p.E18K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371419
Start	54214389:54214389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.63A>C
AA Mutation	p.Gln21His(p.Q21H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371419
Start	54219022:54219022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277A>C
AA Mutation	p.Asn93His(p.N93H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371419
Start	54215329:54215329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.162T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PFDN4

No Mutation Annotation!