Mutation

Primary Site >> Stomach Cancer

Gene >> PTGFR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370757
Start	78492814:78492814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71C>T
AA Mutation	p.Thr24Met(p.T24M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370757
Start	78492814:78492814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71C>A
AA Mutation	p.Thr24Lys(p.T24K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370757
Start	78493510:78493510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767G>A
AA Mutation	p.Cys256Tyr(p.C256Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370757
Start	78493219:78493219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780419713
CDS Mutation	c.476T>C
AA Mutation	p.Val159Ala(p.V159A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370757
Start	78492822:78492822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749469257
CDS Mutation	c.79C>T
AA Mutation	p.Arg27Trp(p.R27W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370757
Start	78493286:78493286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775712841
CDS Mutation	c.543G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370757
Start	78492938:78492938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774495214
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370757
Start	78493400:78493400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370757
Start	78493469:78493469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370757
Start	78492834:78492834(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.97delT
AA Mutation	p.Ser33GlnfsTer2(p.S33Qfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript