Colon Cancer: Gene >> PRIM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338193
Start	56744080:56744080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623T>A
AA Mutation	p.Ile208Asn(p.I208N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338193
Start	56734230:56734230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160G>A
AA Mutation	p.Ser387Asn(p.S387N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338193
Start	56744071:56744071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632T>G
AA Mutation	p.Phe211Cys(p.F211C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338193
Start	56751056:56751056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769305467
CDS Mutation	c.243C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338193
Start	56746104:56746117(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.507_520delCTGTGATGAATCAG
AA Mutation	p.Cys170Ter(p.C170*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338193
Start	56743072:56743072(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.663delA
AA Mutation	p.Lys221AsnfsTer24(p.K221Nfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRIM1

No Mutation Annotation!