Mutation

Primary Site >> Stomach Cancer

Gene >> PARP4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24443708:24443708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200183289
CDS Mutation	c.3389G>A
AA Mutation	p.Arg1130Gln(p.R1130Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24493682:24493682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113456081
CDS Mutation	c.793G>A
AA Mutation	p.Asp265Asn(p.D265N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381989
Start	24452407:24452407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139789669
CDS Mutation	c.3013G>A
AA Mutation	p.Gly1005Ser(p.G1005S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24426518:24426518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4927G>C
AA Mutation	p.Glu1643Gln(p.E1643Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24455070:24455070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758277432
CDS Mutation	c.2705C>T
AA Mutation	p.Ala902Val(p.A902V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24493607:24493607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868A>C
AA Mutation	p.Ser290Arg(p.S290R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24456385:24456385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2518C>T
AA Mutation	p.Leu840Phe(p.L840F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381989
Start	24475595:24475595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1791T>G
AA Mutation	p.Asp597Glu(p.D597E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24492489:24492489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985C>G
AA Mutation	p.Pro329Ala(p.P329A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24501731:24501731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236A>G
AA Mutation	p.Lys79Arg(p.K79R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24503674:24503674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772783590
CDS Mutation	c.103G>A
AA Mutation	p.Gly35Arg(p.G35R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24486219:24486219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1301G>T
AA Mutation	p.Arg434Met(p.R434M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24434892:24434892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4249C>T
AA Mutation	p.Pro1417Ser(p.P1417S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381989
Start	24434395:24434395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4746G>T
AA Mutation	p.Glu1582Asp(p.E1582D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381989
Start	24456344:24456344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771263287
CDS Mutation	c.2559C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381989
Start	24435091:24435091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145651021
CDS Mutation	c.4050C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381989
Start	24498224:24498224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381989
Start	24492552:24492552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.922C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381989
Start	24501700:24501700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381989
Start	24456362:24456362(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2541delA
AA Mutation	p.Lys847AsnfsTer25(p.K847Nfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript