Mutation

Primary Site >> Stomach Cancer

Gene >> CASQ1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368078
Start	160195508:160195508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625C>A
AA Mutation	p.Pro209Thr(p.P209T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368078
Start	160195489:160195489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606G>T
AA Mutation	p.Glu202Asp(p.E202D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368078
Start	160190990:160190990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239C>T
AA Mutation	p.Ala80Val(p.A80V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368078
Start	160195055:160195055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509T>C
AA Mutation	p.Leu170Pro(p.L170P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000368078
Start	160197569:160197569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.783A>T
AA Mutation	p.Arg261Ser(p.R261S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368078
Start	160198967:160198967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898T>G
AA Mutation	p.Leu300Val(p.L300V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368078
Start	160190797:160190797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371555372
CDS Mutation	c.46C>T
AA Mutation	p.Arg16Trp(p.R16W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368078
Start	160201358:160201358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1173C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368078
Start	160199046:160199047(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.982dupC
AA Mutation	p.Leu328ProfsTer11(p.L328Pfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript