Mutation

Primary Site >> Stomach Cancer

Gene >> PAPPA

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116335053:116335053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3590C>T
AA Mutation	p.Thr1197Ile(p.T1197I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116188058:116188058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1320C>G
AA Mutation	p.Cys440Trp(p.C440W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116227464:116227464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2145A>T
AA Mutation	p.Glu715Asp(p.E715D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116332385:116332385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3314C>T
AA Mutation	p.Thr1105Met(p.T1105M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116332429:116332429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3358G>A
AA Mutation	p.Val1120Met(p.V1120M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116352904:116352904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764379532
CDS Mutation	c.4163G>A
AA Mutation	p.Arg1388Gln(p.R1388Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116211654:116211654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1640A>C
AA Mutation	p.Asn547Thr(p.N547T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116211867:116211867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1853G>T
AA Mutation	p.Gly618Val(p.G618V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116344659:116344659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142176678
CDS Mutation	c.3728G>A
AA Mutation	p.Arg1243Gln(p.R1243Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116332387:116332387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3316G>A
AA Mutation	p.Asp1106Asn(p.D1106N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116187304:116187304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374109701
CDS Mutation	c.566G>A
AA Mutation	p.Arg189His(p.R189H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116187407:116187407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669A>C
AA Mutation	p.Gln223His(p.Q223H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116332361:116332361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3290C>T
AA Mutation	p.Ala1097Val(p.A1097V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116187807:116187807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375396659
CDS Mutation	c.1069G>A
AA Mutation	p.Val357Met(p.V357M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116187829:116187829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749158982
CDS Mutation	c.1091A>G
AA Mutation	p.Asp364Gly(p.D364G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116188024:116188024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286A>G
AA Mutation	p.Asn429Ser(p.N429S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116187723:116187723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985C>G
AA Mutation	p.Gln329Glu(p.Q329E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116187243:116187243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772431336
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Cys(p.R169C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116352709:116352709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3968A>G
AA Mutation	p.Asn1323Ser(p.N1323S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000328252
Start	116362608:116362608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4364T>C
AA Mutation	p.Val1455Ala(p.V1455A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116227446:116227446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2127A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116211787:116211787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1773G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116352812:116352812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4071C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116367748:116367748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4599G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116211682:116211682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1668C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116353670:116353670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4224A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116347166:116347166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3921C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116188019:116188019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1281G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116187854:116187854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201148082
CDS Mutation	c.1116C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116188100:116188100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139489198
CDS Mutation	c.1362C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116211853:116211853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1839T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328252
Start	116271346:116271346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751713023
CDS Mutation	c.2883C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328252
Start	116382484:116382484(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4767delG
AA Mutation	p.Thr1590ProfsTer59(p.T1590Pfs*59)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328252
Start	116187196:116187196(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.460delG
AA Mutation	p.Val154SerfsTer21(p.V154Sfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000328252
Start	116211910:116211910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1896C>G
AA Mutation	p.Tyr632Ter(p.Y632*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000328252
Start	116344630:116344630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3699C>A
AA Mutation	p.Tyr1233Ter(p.Y1233*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000328252
Start	116211737:116211737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143947880
CDS Mutation	c.1723C>T
AA Mutation	p.Arg575Ter(p.R575*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000328252
Start	116352828:116352828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4087C>T
AA Mutation	p.Arg1363Ter(p.R1363*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000328252
Start	116367733:116367733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4584G>A
AA Mutation	p.Trp1528Ter(p.W1528*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328252
Start	116302813:116302814(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3016dupA
AA Mutation	p.Thr1006AsnfsTer4(p.T1006Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328252
Start	116335045:116335046(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3586dupG
AA Mutation	p.Glu1196GlyfsTer16(p.E1196Gfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript