Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PDGFC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156767929:156767929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765C>A
AA Mutation	p.Phe255Leu(p.F255L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156970887:156970887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.17T>G
AA Mutation	p.Leu6Arg(p.L6R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156772797:156772797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592G>A
AA Mutation	p.Asp198Asn(p.D198N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502773
Start	156763111:156763111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000502773
Start	156772856:156772856(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.533delC
AA Mutation	p.Pro178LeufsTer13(p.P178Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	start_lost
Transcription ID	ENST00000502773
Start	156970902:156970902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2T>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PDGFC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156850392:156850392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143G>T
AA Mutation	p.Arg48Ile(p.R48I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156850392:156850392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.143G>A
AA Mutation	p.Arg48Lys(p.R48K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156772691:156772691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.698C>A
AA Mutation	p.Ser233Tyr(p.S233Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502773
Start	156772738:156772738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.651G>A
Mutation Classification	Silent
Feature Type	Transcript