Mutation

Primary Site >> Stomach Cancer

Gene >> KAT2A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225916
Start	42114943:42114943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1968T>A
AA Mutation	p.Asn656Lys(p.N656K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225916
Start	42117779:42117779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782708792
CDS Mutation	c.1327G>A
AA Mutation	p.Glu443Lys(p.E443K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225916
Start	42119351:42119351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967C>T
AA Mutation	p.Arg323Trp(p.R323W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225916
Start	42113740:42113740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2423A>G
AA Mutation	p.Asn808Ser(p.N808S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225916
Start	42120710:42120710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.459C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225916
Start	42114521:42114521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2103G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225916
Start	42113748:42113748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200570403
CDS Mutation	c.2415C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225916
Start	42119686:42119690(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.728_732delTTAGT
AA Mutation	p.Phe243SerfsTer22(p.F243Sfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225916
Start	42119390:42119390(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.928delC
AA Mutation	p.Arg310AlafsTer110(p.R310Afs*110)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript