Mutation

Primary Site >> Stomach Cancer

Gene >> NRP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33213409:33213409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1591G>C
AA Mutation	p.Asp531His(p.D531H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33180254:33180254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2594G>A
AA Mutation	p.Ser865Asn(p.S865N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33226241:33226241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771071490
CDS Mutation	c.1030G>A
AA Mutation	p.Ala344Thr(p.A344T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33263798:33263798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506A>G
AA Mutation	p.Asn169Ser(p.N169S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33192329:33192329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2014A>G
AA Mutation	p.Lys672Glu(p.K672E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33213390:33213390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760427841
CDS Mutation	c.1610C>T
AA Mutation	p.Ala537Val(p.A537V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33186329:33186329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554872876
CDS Mutation	c.2222G>A
AA Mutation	p.Arg741His(p.R741H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33202933:33202933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1822G>A
AA Mutation	p.Ala608Thr(p.A608T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33270683:33270683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.422T>C
AA Mutation	p.Phe141Ser(p.F141S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33180359:33180359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750320738
CDS Mutation	c.2489C>T
AA Mutation	p.Thr830Met(p.T830M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33330817:33330817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139T>A
AA Mutation	p.Ser47Thr(p.S47T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33192406:33192406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770248476
CDS Mutation	c.1937A>G
AA Mutation	p.Tyr646Cys(p.Y646C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265371
Start	33202940:33202940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148913335
CDS Mutation	c.1815C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265371
Start	33226191:33226191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139187411
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265371
Start	33207615:33207615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1716C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265371
Start	33256388:33256388(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.742delT
AA Mutation	p.Tyr248ThrfsTer6(p.Y248Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000265371
Start	33213548:33213548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1452G>A
AA Mutation	p.Trp484Ter(p.W484*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000265371
Start	33256427:33256427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703C>T
AA Mutation	p.Arg235Ter(p.R235*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000265371
Start	33256421:33256421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Ter(p.R237*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript