Mutation

Primary Site >> Stomach Cancer

Gene >> CLK2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155269525:155269525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201854491
CDS Mutation	c.362G>A
AA Mutation	p.Arg121Gln(p.R121Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155263313:155263313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1405A>G
AA Mutation	p.Thr469Ala(p.T469A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155270892:155270892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86G>A
AA Mutation	p.Arg29Gln(p.R29Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000368361
Start	155263952:155263952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315C>T
AA Mutation	p.Arg439Trp(p.R439W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155264512:155264512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102G>T
AA Mutation	p.Gly368Cys(p.G368C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155263277:155263277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771821636
CDS Mutation	c.1441C>T
AA Mutation	p.Arg481Cys(p.R481C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155268098:155268098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583A>G
AA Mutation	p.Ile195Val(p.I195V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155265889:155265889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904G>C
AA Mutation	p.Asp302His(p.D302H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155263973:155263973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759554148
CDS Mutation	c.1294C>T
AA Mutation	p.Arg432Cys(p.R432C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155264665:155264665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1043G>A
AA Mutation	p.Arg348Gln(p.R348Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155263280:155263280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746962823
CDS Mutation	c.1438G>A
AA Mutation	p.Ala480Thr(p.A480T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155264770:155264770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.938G>T
AA Mutation	p.Arg313Leu(p.R313L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000368361
Start	155263319:155263319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1399C>T
AA Mutation	p.Arg467Trp(p.R467W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368361
Start	155269668:155269668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368361
Start	155263317:155263317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1401G>A
Mutation Classification	Silent
Feature Type	Transcript