Mutation

Primary Site >> Stomach Cancer

Gene >> ATN1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6938614:6938614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2651G>A
AA Mutation	p.Arg884His(p.R884H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6941009:6941009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782023721
CDS Mutation	c.3344G>A
AA Mutation	p.Arg1115His(p.R1115H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6936600:6936600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1333C>T
AA Mutation	p.Pro445Ser(p.P445S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6934240:6934240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92G>A
AA Mutation	p.Gly31Asp(p.G31D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6938794:6938794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2831A>G
AA Mutation	p.Asp944Gly(p.D944G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6936072:6936072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781823465
CDS Mutation	c.805G>A
AA Mutation	p.Gly269Ser(p.G269S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6941476:6941476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3461C>T
AA Mutation	p.Ala1154Val(p.A1154V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356654
Start	6935669:6935669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356654
Start	6935810:6935810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356654
Start	6937118:6937118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1851C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356654
Start	6937139:6937139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1872G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356654
Start	6937115:6937115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781947193
CDS Mutation	c.1848G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356654
Start	6936227:6936227(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.964delG
AA Mutation	p.Ala322ProfsTer50(p.A322Pfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356654
Start	6936026:6936026(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.764delC
AA Mutation	p.Pro255HisfsTer43(p.P255Hfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356654
Start	6936537:6936537(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs782523332
CDS Mutation	c.1275delC
AA Mutation	p.Lys426SerfsTer27(p.K426Sfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356654
Start	6936372:6936372(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1110delC
AA Mutation	p.Met371Ter(p.M371*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356654
Start	6936078:6936078(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.815delC
AA Mutation	p.Pro272GlnfsTer26(p.P272Qfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356654
Start	6935864:6935865(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.603dupC
AA Mutation	p.Thr202HisfsTer47(p.T202Hfs*47)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript