Mutation

Primary Site >> Stomach Cancer

Gene >> PDGFC

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156850285:156850285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250G>A
AA Mutation	p.Val84Ile(p.V84I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156763152:156763152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150603208
CDS Mutation	c.976G>A
AA Mutation	p.Asp326Asn(p.D326N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156767792:156767792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902T>C
AA Mutation	p.Val301Ala(p.V301A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156763181:156763181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Gly316Asp(p.G316D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156850292:156850292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243G>T
AA Mutation	p.Glu81Asp(p.E81D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000502773
Start	156772743:156772743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646T>C
AA Mutation	p.Tyr216His(p.Y216H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502773
Start	156763150:156763150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769405300
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502773
Start	156850337:156850337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502773
Start	156810942:156810942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000502773
Start	156767782:156767782(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.912delA
AA Mutation	p.Lys304AsnfsTer8(p.K304Nfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript