Mutation

Primary Site >> Stomach Cancer

Gene >> DLX6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000518156
Start	97009820:97009820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655C>T
AA Mutation	p.Arg219Cys(p.R219C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000518156
Start	97009858:97009858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693T>A
AA Mutation	p.Asn231Lys(p.N231K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000518156
Start	97009899:97009899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530888638
CDS Mutation	c.734C>T
AA Mutation	p.Ser245Leu(p.S245L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518156
Start	97009900:97009900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760073542
CDS Mutation	c.735G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518156
Start	97009825:97009825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.660T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518156
Start	97009891:97009891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766818524
CDS Mutation	c.726G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518156
Start	97009945:97009945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377688666
CDS Mutation	c.780G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518156
Start	97009870:97009870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371198246
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000518156
Start	97009873:97009873(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.712delC
AA Mutation	p.Leu238SerfsTer55(p.L238Sfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000518156
Start	97009963:97009964(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.804dupC
AA Mutation	p.Asn269GlnfsTer59(p.N269Qfs*59)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript