Mutation

Primary Site >> Stomach Cancer

Gene >> PDGFD

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393158
Start	103927096:103927096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138058754
CDS Mutation	c.803A>G
AA Mutation	p.Lys268Arg(p.K268R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393158
Start	104000235:104000235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.145T>G
AA Mutation	p.Leu49Val(p.L49V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393158
Start	103943463:103943463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147536650
CDS Mutation	c.761G>A
AA Mutation	p.Arg254Gln(p.R254Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393158
Start	103909716:103909716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091G>A
AA Mutation	p.Cys364Tyr(p.C364Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393158
Start	103926997:103926997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771113435
CDS Mutation	c.902G>A
AA Mutation	p.Arg301His(p.R301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393158
Start	103943587:103943587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637A>C
AA Mutation	p.Lys213Gln(p.K213Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000393158
Start	103909773:103909773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034A>G
AA Mutation	p.Lys345Arg(p.K345R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393158
Start	103943621:103943621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776396736
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393158
Start	104000197:104000197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148454316
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393158
Start	104163853:104163853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769507921
CDS Mutation	c.75G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393158
Start	103996143:103996143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393158
Start	103943584:103943584(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.640delA
AA Mutation	p.Ile214LeufsTer68(p.I214Lfs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393158
Start	103926922:103926922(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.977delA
AA Mutation	p.Lys326SerfsTer24(p.K326Sfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000393158
Start	103996214:103996214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>T
AA Mutation	p.Glu121Ter(p.E121*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000393158
Start	103996063:103996063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript