Mutation

Primary Site >> Stomach Cancer

Gene >> PARP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366794
Start	226381103:226381103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751338176
CDS Mutation	c.1265C>T
AA Mutation	p.Thr422Met(p.T422M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366794
Start	226374329:226374329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1967C>T
AA Mutation	p.Thr656Ile(p.T656I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366794
Start	226379212:226379212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1675C>A
AA Mutation	p.Leu559Met(p.L559M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366794
Start	226383102:226383102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774530658
CDS Mutation	c.1093G>A
AA Mutation	p.Val365Met(p.V365M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366794
Start	226381139:226381139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1229C>T
AA Mutation	p.Ala410Val(p.A410V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366794
Start	226381109:226381109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757100394
CDS Mutation	c.1259C>T
AA Mutation	p.Thr420Met(p.T420M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366794
Start	226366037:226366037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2422T>A
AA Mutation	p.Ser808Thr(p.S808T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000366794
Start	226374297:226374297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1999A>G
AA Mutation	p.Lys667Glu(p.K667E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000366794
Start	226379924:226379924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1541A>G
AA Mutation	p.Glu514Gly(p.E514G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000366794
Start	226377278:226377278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752905479
CDS Mutation	c.1771C>T
AA Mutation	p.Arg591Cys(p.R591C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000366794
Start	226365121:226365121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750773674
CDS Mutation	c.2539C>T
AA Mutation	p.Arg847Cys(p.R847C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366794
Start	226385597:226385597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755443483
CDS Mutation	c.918C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366794
Start	226365131:226365131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148631906
CDS Mutation	c.2529C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366794
Start	226381174:226381174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373462891
CDS Mutation	c.1194C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366794
Start	226363139:226363139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2808A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366794
Start	226368250:226368250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761046396
CDS Mutation	c.2226C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366794
Start	226388743:226388743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372233336
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366794
Start	226379946:226379946(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1519delA
AA Mutation	p.Ser507AlafsTer17(p.S507Afs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366794
Start	226368261:226368261(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2215delC
AA Mutation	p.Leu739Ter(p.L739*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366794
Start	226383139:226383139(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1056delA
AA Mutation	p.Lys352AsnfsTer29(p.K352Nfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript