Mutation

Primary Site >> Stomach Cancer

Gene >> NHS

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17726652:17726652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2483C>T
AA Mutation	p.Pro828Leu(p.P828L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17725574:17725574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1405G>A
AA Mutation	p.Gly469Ser(p.G469S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17726711:17726711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748302530
CDS Mutation	c.2542G>A
AA Mutation	p.Glu848Lys(p.E848K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17727480:17727480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145005596
CDS Mutation	c.3311C>T
AA Mutation	p.Ser1104Leu(p.S1104L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17687747:17687747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.571T>C
AA Mutation	p.Ser191Pro(p.S191P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17732379:17732379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367919114
CDS Mutation	c.4808C>T
AA Mutation	p.Thr1603Met(p.T1603M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17725949:17725949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767956070
CDS Mutation	c.1780G>A
AA Mutation	p.Val594Ile(p.V594I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17721565:17721565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200668785
CDS Mutation	c.977C>T
AA Mutation	p.Thr326Met(p.T326M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17726153:17726153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587780403
CDS Mutation	c.1984G>A
AA Mutation	p.Val662Met(p.V662M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17725848:17725848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1679G>A
AA Mutation	p.Arg560Lys(p.R560K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17726034:17726034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1865C>T
AA Mutation	p.Ser622Leu(p.S622L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17725890:17725890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1721A>G
AA Mutation	p.Asp574Gly(p.D574G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17727587:17727587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3418G>A
AA Mutation	p.Asp1140Asn(p.D1140N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000380060
Start	17728697:17728697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4208C>A
AA Mutation	p.Ser1403Tyr(p.S1403Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17687788:17687788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777799752
CDS Mutation	c.612C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17727691:17727691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3522T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17727706:17727706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3537G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17721509:17721509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17726419:17726419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758417770
CDS Mutation	c.2250G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17726926:17726926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2757C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380060
Start	17726269:17726269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2100T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380060
Start	17692377:17692377(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.766delC
AA Mutation	p.Leu256PhefsTer28(p.L256Ffs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000380060
Start	17732387:17732387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4816C>T
AA Mutation	p.Gln1606Ter(p.Q1606*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript