Mutation

Primary Site >> Stomach Cancer

Gene >> KCNA6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4811083:4811083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Trp(p.R348W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4811306:4811306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1265C>T
AA Mutation	p.Thr422Met(p.T422M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4811230:4811230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1189G>T
AA Mutation	p.Ala397Ser(p.A397S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4810513:4810513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.472C>T
AA Mutation	p.Arg158Cys(p.R158C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4811360:4811360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1319C>T
AA Mutation	p.Ser440Leu(p.S440L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4810324:4810324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Ala95Thr(p.A95T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4810192:4810192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.151C>T
AA Mutation	p.Arg51Cys(p.R51C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4811249:4811249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1208A>G
AA Mutation	p.Asp403Gly(p.D403G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4810088:4810088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>A
AA Mutation	p.Arg16His(p.R16H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4810907:4810907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866C>T
AA Mutation	p.Pro289Leu(p.P289L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4811396:4811396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1355T>C
AA Mutation	p.Leu452Pro(p.L452P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4810115:4810115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770209419
CDS Mutation	c.74C>T
AA Mutation	p.Ala25Val(p.A25V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4810094:4810094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778808157
CDS Mutation	c.53C>T
AA Mutation	p.Pro18Leu(p.P18L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4810355:4810355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314G>A
AA Mutation	p.Arg105His(p.R105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4811075:4811075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1034G>A
AA Mutation	p.Arg345His(p.R345H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4810759:4810759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.718C>T
AA Mutation	p.Pro240Ser(p.P240S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000280684
Start	4811369:4811369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1328C>T
AA Mutation	p.Ala443Val(p.A443V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280684
Start	4811499:4811499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200395161
CDS Mutation	c.1458G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280684
Start	4810074:4810074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280684
Start	4810845:4810845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280684
Start	4810353:4810353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280684
Start	4811361:4811361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750929085
CDS Mutation	c.1320G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280684
Start	4810137:4810137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.96C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280684
Start	4811406:4811406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1365C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280684
Start	4810275:4810275(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.238delC
AA Mutation	p.Leu80Ter(p.L80*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280684
Start	4810804:4810804(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.767delG
AA Mutation	p.Gly256AlafsTer41(p.G256Afs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript