Mutation

Primary Site >> Stomach Cancer

Gene >> GAB2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361507
Start	78219287:78219287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2016G>T
AA Mutation	p.Lys672Asn(p.K672N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361507
Start	78226503:78226503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750289098
CDS Mutation	c.1169A>G
AA Mutation	p.Asn390Ser(p.N390S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361507
Start	78226722:78226722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116286425
CDS Mutation	c.950C>T
AA Mutation	p.Pro317Leu(p.P317L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361507
Start	78223417:78223417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1562G>A
AA Mutation	p.Arg521Gln(p.R521Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361507
Start	78222161:78222161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361507
Start	78219314:78219314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145964223
CDS Mutation	c.1989C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361507
Start	78225117:78225117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1293C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361507
Start	78250216:78250216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361507
Start	78223515:78223515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1464A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361507
Start	78250242:78250255(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.522_535delCCCTGTGTCAAACC
AA Mutation	p.Pro175HisfsTer45(p.P175Hfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript