Mutation

Primary Site >> Stomach Cancer

Gene >> GAA

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80105812:80105812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780799275
CDS Mutation	c.610G>A
AA Mutation	p.Ala204Thr(p.A204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80112929:80112929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536906561
CDS Mutation	c.1942G>A
AA Mutation	p.Gly648Ser(p.G648S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000302262
Start	80117108:80117108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746779016
CDS Mutation	c.2330C>T
AA Mutation	p.Thr777Met(p.T777M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000302262
Start	80112580:80112580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770021831
CDS Mutation	c.1757C>T
AA Mutation	p.Ala586Val(p.A586V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80108712:80108712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141533320
CDS Mutation	c.1210G>A
AA Mutation	p.Asp404Asn(p.D404N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302262
Start	80113293:80113293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2116C>A
AA Mutation	p.Leu706Ile(p.L706I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302262
Start	80117052:80117052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150431943
CDS Mutation	c.2274C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302262
Start	80107841:80107841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302262
Start	80117686:80117686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371528938
CDS Mutation	c.2418G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302262
Start	80112913:80112913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1926C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302262
Start	80104904:80104904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762542246
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302262
Start	80117630:80117630(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2366delC
AA Mutation	p.Pro789HisfsTer17(p.P789Hfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302262
Start	80117015:80117015(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2242delG
AA Mutation	p.Glu748ArgfsTer16(p.E748Rfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302262
Start	80104838:80104838(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.258delC
AA Mutation	p.Asn87ThrfsTer55(p.N87Tfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript