Mutation

Primary Site >> Stomach Cancer

Gene >> DAPK1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87686658:87686658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2332G>T
AA Mutation	p.Val778Leu(p.V778L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87650030:87650030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778729228
CDS Mutation	c.1538C>T
AA Mutation	p.Thr513Met(p.T513M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87706222:87706222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368803870
CDS Mutation	c.3151G>A
AA Mutation	p.Val1051Met(p.V1051M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87707015:87707015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368364961
CDS Mutation	c.3944G>A
AA Mutation	p.Arg1315His(p.R1315H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87707291:87707291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4220G>A
AA Mutation	p.Gly1407Asp(p.G1407D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87706471:87706471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3400G>A
AA Mutation	p.Val1134Met(p.V1134M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87648796:87648796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1345C>A
AA Mutation	p.Leu449Ile(p.L449I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87650013:87650013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1521G>T
AA Mutation	p.Lys507Asn(p.K507N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87668622:87668622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1949C>T
AA Mutation	p.Ala650Val(p.A650V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87698781:87698781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2737G>C
AA Mutation	p.Glu913Gln(p.E913Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000358077
Start	87639355:87639355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425C>A
AA Mutation	p.Pro142His(p.P142H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87700164:87700164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2798C>T
AA Mutation	p.Ala933Val(p.A933V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87651646:87651646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1746T>A
AA Mutation	p.His582Gln(p.H582Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87647335:87647335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1261C>T
AA Mutation	p.Arg421Trp(p.R421W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000358077
Start	87706525:87706525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3454C>A
AA Mutation	p.Leu1152Met(p.L1152M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358077
Start	87706815:87706815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3744C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358077
Start	87703040:87703040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2883C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358077
Start	87668608:87668608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773785893
CDS Mutation	c.1935G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358077
Start	87698771:87698771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371785798
CDS Mutation	c.2727G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358077
Start	87706464:87706464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765353398
CDS Mutation	c.3393C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358077
Start	87640403:87640403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358077
Start	87649931:87649931(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1444delC
AA Mutation	p.Leu482CysfsTer23(p.L482Cfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358077
Start	87706887:87706887(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3822delG
AA Mutation	p.Tyr1275ThrfsTer31(p.Y1275Tfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358077
Start	87697196:87697196(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2604delA
AA Mutation	p.Glu868AspfsTer3(p.E868Dfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358077
Start	87637988:87637989(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.331_332delTT
AA Mutation	p.Leu111AsnfsTer2(p.L111Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358077
Start	87639453:87639453(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.527delA
AA Mutation	p.Asn176ThrfsTer13(p.N176Tfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000358077
Start	87650009:87650035(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1519_1545delAAGAACCGAGAAGGAGAGACGCCCCTC
AA Mutation	p.Lys507_Leu515del(p.K507_L515del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript