Mutation

Primary Site >> Stomach Cancer

Gene >> AOAH

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000617537
Start	36637906:36637906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.395C>T
AA Mutation	p.Thr132Ile(p.T132I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000617537
Start	36532149:36532149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1423G>A
AA Mutation	p.Glu475Lys(p.E475K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000617537
Start	36673956:36673956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277G>T
AA Mutation	p.Asp93Tyr(p.D93Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000617537
Start	36673979:36673979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254T>C
AA Mutation	p.Leu85Ser(p.L85S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617537
Start	36632068:36632068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553727878
CDS Mutation	c.489G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617537
Start	36637857:36637857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764322776
CDS Mutation	c.444G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617537
Start	36724068:36724068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762691800
CDS Mutation	c.81C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617537
Start	36540443:36540443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000617537
Start	36621713:36621725(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.638_650delTGTACCCAGGTAG
AA Mutation	p.Val213GlufsTer66(p.V213Efs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript