Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SERPING1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278407
Start	57600165:57600165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338C>A
AA Mutation	p.Ser113Tyr(p.S113Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278407
Start	57614339:57614339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1261T>G
AA Mutation	p.Phe421Val(p.F421V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278407
Start	57606205:57606205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.881A>G
AA Mutation	p.Tyr294Cys(p.Y294C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278407
Start	57600293:57600293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139035354
CDS Mutation	c.466G>A
AA Mutation	p.Ala156Thr(p.A156T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278407
Start	57599992:57599992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278407
Start	57614542:57614542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1464C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278407
Start	57606092:57606092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146449093
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278407
Start	57606045:57606045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278407
Start	57611881:57611882(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1198dupC
AA Mutation	p.Arg400ProfsTer25(p.R400Pfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SERPING1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278407
Start	57611885:57611885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201363394
CDS Mutation	c.1198C>T
AA Mutation	p.Arg400Cys(p.R400C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278407
Start	57600165:57600165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338C>A
AA Mutation	p.Ser113Tyr(p.S113Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278407
Start	57599952:57599952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125A>G
AA Mutation	p.Glu42Gly(p.E42G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278407
Start	57602119:57602119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635G>A
AA Mutation	p.Gly212Asp(p.G212D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278407
Start	57611767:57611767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript