Mutation

Primary Site >> Stomach Cancer

Gene >> DCLK1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35805775:35805775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1868T>A
AA Mutation	p.Leu623His(p.L623H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36112181:36112181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411C>G
AA Mutation	p.Phe137Leu(p.F137L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36111918:36111918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.674A>C
AA Mutation	p.Lys225Thr(p.K225T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35822835:35822835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1448A>G
AA Mutation	p.Tyr483Cys(p.Y483C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36126005:36126005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133C>T
AA Mutation	p.Arg45Cys(p.R45C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36125900:36125900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238C>T
AA Mutation	p.Arg80Trp(p.R80W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35871241:35871241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923C>G
AA Mutation	p.Pro308Arg(p.P308R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36112119:36112119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.473C>G
AA Mutation	p.Ser158Trp(p.S158W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35836135:35836135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754265976
CDS Mutation	c.1127C>T
AA Mutation	p.Ser376Leu(p.S376L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36112145:36112145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.447C>A
AA Mutation	p.Asn149Lys(p.N149K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35810946:35810946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1577G>A
AA Mutation	p.Ser526Asn(p.S526N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36126029:36126029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760301962
CDS Mutation	c.109G>A
AA Mutation	p.Ala37Thr(p.A37T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36125834:36125834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304C>T
AA Mutation	p.Pro102Ser(p.P102S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35854524:35854524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010G>T
AA Mutation	p.Ser337Ile(p.S337I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36112161:36112161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431A>G
AA Mutation	p.Lys144Arg(p.K144R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35805764:35805764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1879A>G
AA Mutation	p.Met627Val(p.M627V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35871259:35871259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905C>A
AA Mutation	p.Ser302Tyr(p.S302Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35774657:35774657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2101C>T
AA Mutation	p.Arg701Cys(p.R701C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36125899:36125899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239G>A
AA Mutation	p.Arg80Gln(p.R80Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35947398:35947398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.783G>T
AA Mutation	p.Glu261Asp(p.E261D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35805713:35805713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1930C>A
AA Mutation	p.His644Asn(p.H644N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35947396:35947396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785A>C
AA Mutation	p.Lys262Thr(p.K262T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36112047:36112047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545T>C
AA Mutation	p.Phe182Ser(p.F182S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36125777:36125777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>T
AA Mutation	p.Asp121Tyr(p.D121Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35836085:35836085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177G>A
AA Mutation	p.Gly393Arg(p.G393R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35793439:35793439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1985C>G
AA Mutation	p.Ala662Gly(p.A662G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35810934:35810934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1589A>C
AA Mutation	p.Lys530Thr(p.K530T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35947435:35947435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746T>G
AA Mutation	p.Phe249Cys(p.F249C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36126085:36126085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53C>T
AA Mutation	p.Ala18Val(p.A18V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36126095:36126095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43C>T
AA Mutation	p.Arg15Trp(p.R15W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36111886:36111886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706A>G
AA Mutation	p.Thr236Ala(p.T236A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	35871247:35871247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.917A>G
AA Mutation	p.Lys306Arg(p.K306R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36125791:36125791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764457570
CDS Mutation	c.347A>G
AA Mutation	p.Lys116Arg(p.K116R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000360631
Start	35827754:35827754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773811526
CDS Mutation	c.1288G>A
AA Mutation	p.Glu430Lys(p.E430K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36112111:36112111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368906217
CDS Mutation	c.481C>T
AA Mutation	p.Arg161Trp(p.R161W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36126001:36126001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137C>T
AA Mutation	p.Thr46Met(p.T46M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36112029:36112029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563T>C
AA Mutation	p.Val188Ala(p.V188A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36125858:36125858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280A>C
AA Mutation	p.Thr94Pro(p.T94P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000360631
Start	36111894:36111894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.698G>A
AA Mutation	p.Arg233His(p.R233H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360631
Start	35809053:35809053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360631
Start	35822822:35822822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201558028
CDS Mutation	c.1461C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360631
Start	36125937:36125937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360631
Start	36112115:36112115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360631
Start	35827728:35827728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1314T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360631
Start	35871258:35871258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.906C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360631
Start	36125850:36125850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767064135
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360631
Start	36125934:36125934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201694528
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360631
Start	36111896:36111896(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.696delA
AA Mutation	p.Lys232AsnfsTer11(p.K232Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	49
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360631
Start	35871305:35871305(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.859delA
AA Mutation	p.Ile287Ter(p.I287*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	50
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360631
Start	35822871:35822871(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1412delG
AA Mutation	p.Gly471GlufsTer25(p.G471Efs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	51
Mutation Consequence	stop_gained
Transcription ID	ENST00000360631
Start	35871335:35871335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829C>T
AA Mutation	p.Arg277Ter(p.R277*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	52
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360631
Start	35854504:35854505(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1029_1030insGG
AA Mutation	p.Gln344GlyfsTer44(p.Q344Gfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360631
Start	35947433:35947434(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.747dupT
AA Mutation	p.Gly250TrpfsTer2(p.G250Wfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	54
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360631
Start	36125904:36125905(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.233dupC
AA Mutation	p.Asp79ArgfsTer7(p.D79Rfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript