Mutation

Primary Site >> Stomach Cancer

Gene >> KCNB1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49373326:49373326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2234C>T
AA Mutation	p.Ala745Val(p.A745V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49482015:49482015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466C>T
AA Mutation	p.Arg156Trp(p.R156W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374679:49374679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779573636
CDS Mutation	c.881G>A
AA Mutation	p.Arg294His(p.R294H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374644:49374644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Cys(p.R306C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49373482:49373482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2078A>T
AA Mutation	p.Asp693Val(p.D693V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49482027:49482027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454G>A
AA Mutation	p.Ala152Thr(p.A152T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49373966:49373966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1594A>G
AA Mutation	p.Met532Val(p.M532V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49482320:49482320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161G>A
AA Mutation	p.Arg54His(p.R54H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374191:49374191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1369A>G
AA Mutation	p.Ser457Gly(p.S457G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374911:49374911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649C>G
AA Mutation	p.Leu217Val(p.L217V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374683:49374683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877C>T
AA Mutation	p.Arg293Cys(p.R293C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49373424:49373424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139458439
CDS Mutation	c.2136G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49373766:49373766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1794C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49373925:49373925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49374720:49374720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748523037
CDS Mutation	c.840C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49373583:49373583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1977T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49374867:49374867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765195036
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49482025:49482025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371741
Start	49373638:49373638(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1922delA
AA Mutation	p.Asn641ThrfsTer21(p.N641Tfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371741
Start	49373020:49373020(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2540delG
AA Mutation	p.Gly847GlufsTer24(p.G847Efs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371741
Start	49373354:49373354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2206delC
AA Mutation	p.Arg736GlyfsTer9(p.R736Gfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript