Mutation

Primary Site >> Stomach Cancer

Gene >> CYTH3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396741
Start	6165560:6165560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.960G>C
AA Mutation	p.Glu320Asp(p.E320D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396741
Start	6165804:6165804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750874462
CDS Mutation	c.833G>A
AA Mutation	p.Arg278His(p.R278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396741
Start	6170559:6170559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781110781
CDS Mutation	c.799C>T
AA Mutation	p.Arg267Cys(p.R267C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396741
Start	6170590:6170590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396741
Start	6170599:6170599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.759C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396741
Start	6171281:6171281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396741
Start	6170857:6170857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199705025
CDS Mutation	c.684C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396741
Start	6164947:6164947(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1200delA
AA Mutation	p.Lys400AsnfsTer6(p.K400Nfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396741
Start	6164946:6164947(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1200dupA
AA Mutation	p.Ter401IlefsTer10(p.401Ifs10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript