Mutation

Primary Site >> Stomach Cancer

Gene >> KCNA4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328224
Start	30011727:30011727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952T>A
AA Mutation	p.Leu318Ile(p.L318I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328224
Start	30010817:30010817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1862C>A
AA Mutation	p.Ser621Tyr(p.S621Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328224
Start	30010910:30010910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1769C>T
AA Mutation	p.Pro590Leu(p.P590L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328224
Start	30011687:30011687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.992A>C
AA Mutation	p.Glu331Ala(p.E331A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328224
Start	30012005:30012005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775798928
CDS Mutation	c.674G>A
AA Mutation	p.Arg225His(p.R225H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328224
Start	30011676:30011676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747595084
CDS Mutation	c.1003G>A
AA Mutation	p.Asp335Asn(p.D335N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328224
Start	30011427:30011427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1252A>G
AA Mutation	p.Thr418Ala(p.T418A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000328224
Start	30012033:30012033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768852661
CDS Mutation	c.646C>T
AA Mutation	p.Arg216Cys(p.R216C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000328224
Start	30011136:30011136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1543T>A
AA Mutation	p.Phe515Ile(p.F515I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000328224
Start	30011130:30011130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1549T>C
AA Mutation	p.Trp517Arg(p.W517R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000328224
Start	30012149:30012149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530G>T
AA Mutation	p.Arg177Leu(p.R177L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328224
Start	30011734:30011734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328224
Start	30011677:30011677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374525769
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328224
Start	30012475:30012475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328224
Start	30012046:30012046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328224
Start	30012016:30012016(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs754892524
CDS Mutation	c.663delT
AA Mutation	p.Phe221LeufsTer21(p.F221Lfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328224
Start	30012512:30012512(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.167delG
AA Mutation	p.Gly56ValfsTer53(p.G56Vfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328224
Start	30011706:30011706(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.973delT
AA Mutation	p.Cys325AlafsTer18(p.C325Afs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328224
Start	30011393:30011393(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1286delG
AA Mutation	p.Gly429ValfsTer53(p.G429Vfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript