Mutation

Primary Site >> Stomach Cancer

Gene >> WSB1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262394
Start	27309224:27309224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774909949
CDS Mutation	c.836G>A
AA Mutation	p.Arg279Gln(p.R279Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262394
Start	27301796:27301796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49C>T
AA Mutation	p.Arg17Cys(p.R17C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262394
Start	27301899:27301899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.152G>C
AA Mutation	p.Trp51Ser(p.W51S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262394
Start	27312335:27312335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1232C>T
AA Mutation	p.Ser411Phe(p.S411F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262394
Start	27303403:27303403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262394
Start	27306867:27306867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778676703
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262394
Start	27303610:27303610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000262394
Start	27310119:27310119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943C>T
AA Mutation	p.Arg315Ter(p.R315*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262394
Start	27303442:27303443(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.290dupA
AA Mutation	p.Asn97LysfsTer2(p.N97Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript