Mutation

Primary Site >> Stomach Cancer

Gene >> KCNB2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72567874:72567874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140A>G
AA Mutation	p.Glu47Gly(p.E47G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72567989:72567989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255C>G
AA Mutation	p.Asn85Lys(p.N85K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72567875:72567875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141A>C
AA Mutation	p.Glu47Asp(p.E47D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72936041:72936041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686A>T
AA Mutation	p.Asp229Val(p.D229V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72936827:72936827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761567231
CDS Mutation	c.1472G>A
AA Mutation	p.Arg491Gln(p.R491Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72568246:72568246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512G>A
AA Mutation	p.Cys171Tyr(p.C171Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72937348:72937348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1993G>T
AA Mutation	p.Gly665Cys(p.G665C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72936360:72936360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005G>T
AA Mutation	p.Leu335Phe(p.L335F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72568045:72568045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311G>A
AA Mutation	p.Arg104Gln(p.R104Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72936854:72936854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1499C>T
AA Mutation	p.Ser500Leu(p.S500L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72937099:72937099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744C>T
AA Mutation	p.Pro582Ser(p.P582S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72936065:72936065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710A>T
AA Mutation	p.Glu237Val(p.E237V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72937223:72937223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370327292
CDS Mutation	c.1868C>T
AA Mutation	p.Pro623Leu(p.P623L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72937231:72937231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139648032
CDS Mutation	c.1876G>A
AA Mutation	p.Ala626Thr(p.A626T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72937153:72937153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1798A>T
AA Mutation	p.Thr600Ser(p.T600S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72936874:72936874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1519T>C
AA Mutation	p.Ser507Pro(p.S507P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72936680:72936680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758557585
CDS Mutation	c.1325G>A
AA Mutation	p.Arg442Gln(p.R442Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72936679:72936679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750665772
CDS Mutation	c.1324C>T
AA Mutation	p.Arg442Trp(p.R442W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72567998:72567998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264C>A
AA Mutation	p.Phe88Leu(p.F88L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72936250:72936250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895G>A
AA Mutation	p.Val299Met(p.V299M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000523207
Start	72937261:72937261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1906G>A
AA Mutation	p.Asp636Asn(p.D636N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523207
Start	72937446:72937446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549207651
CDS Mutation	c.2091C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523207
Start	72568094:72568094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523207
Start	72567965:72567965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523207
Start	72567989:72567989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765881996
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523207
Start	72568025:72568025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523207
Start	72937116:72937116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141923254
CDS Mutation	c.1761C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523207
Start	72937788:72937788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150484780
CDS Mutation	c.2433C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523207
Start	72936819:72936819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201431676
CDS Mutation	c.1464G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523207
Start	72567851:72567851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000523207
Start	72567857:72567857(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.128delG
AA Mutation	p.Gly43AlafsTer40(p.G43Afs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000523207
Start	72937299:72937299(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1949delC
AA Mutation	p.Pro650ArgfsTer3(p.P650Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000523207
Start	72568162:72568162(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs752059864
CDS Mutation	c.435delA
AA Mutation	p.Glu146AsnfsTer3(p.E146Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000523207
Start	72937634:72937634(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2283delC
AA Mutation	p.Ser762ProfsTer46(p.S762Pfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000523207
Start	72567750:72567750(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.20delC
AA Mutation	p.Pro7ArgfsTer3(p.P7Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000523207
Start	72568161:72568162(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.435dupA
AA Mutation	p.Glu146ArgfsTer23(p.E146Rfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	37
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000523207
Start	72568220:72568222(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.488_490delAAG
AA Mutation	p.Glu163del(p.E163del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript