Mutation

Primary Site >> Stomach Cancer

Gene >> KIAA1324

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369939
Start	109164647:109164647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423G>A
AA Mutation	p.Met141Ile(p.M141I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369939
Start	109200229:109200229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2799G>T
AA Mutation	p.Lys933Asn(p.K933N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369939
Start	109198624:109198624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773197105
CDS Mutation	c.2451C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369939
Start	109192724:109192724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1797C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369939
Start	109164644:109164644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369939
Start	109185127:109185127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1035C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369939
Start	109197497:109197497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769086777
CDS Mutation	c.2145C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369939
Start	109200184:109200184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2754T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369939
Start	109192794:109192794(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1867delA
AA Mutation	p.Thr623LeufsTer5(p.T623Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000369939
Start	109191403:109191403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1477G>T
AA Mutation	p.Glu493Ter(p.E493*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript