Mutation

Primary Site >> Stomach Cancer

Gene >> ADAMTS9

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64561727:64561727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4549G>A
AA Mutation	p.Val1517Ile(p.V1517I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64616061:64616061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2923G>T
AA Mutation	p.Val975Phe(p.V975F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64602006:64602006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778701337
CDS Mutation	c.3955G>A
AA Mutation	p.Ala1319Thr(p.A1319T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64594413:64594413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4201G>T
AA Mutation	p.Gly1401Cys(p.G1401C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64541340:64541340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5367C>G
AA Mutation	p.Phe1789Leu(p.F1789L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64546948:64546948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764052034
CDS Mutation	c.4874C>T
AA Mutation	p.Ser1625Leu(p.S1625L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64596961:64596961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758184611
CDS Mutation	c.4048C>T
AA Mutation	p.Arg1350Trp(p.R1350W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64622320:64622320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2564C>T
AA Mutation	p.Ser855Leu(p.S855L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64622445:64622445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148570059
CDS Mutation	c.2531G>A
AA Mutation	p.Arg844His(p.R844H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64622290:64622290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2594G>A
AA Mutation	p.Arg865His(p.R865H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64686608:64686608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476A>C
AA Mutation	p.Asn159Thr(p.N159T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64658593:64658593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772774188
CDS Mutation	c.878G>A
AA Mutation	p.Arg293Gln(p.R293Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000498707
Start	64633474:64633474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374662732
CDS Mutation	c.2173C>T
AA Mutation	p.Arg725Trp(p.R725W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64633728:64633728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767334673
CDS Mutation	c.2008A>G
AA Mutation	p.Asn670Asp(p.N670D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64594424:64594424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4190T>C
AA Mutation	p.Leu1397Pro(p.L1397P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64647959:64647959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1691C>T
AA Mutation	p.Thr564Met(p.T564M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64541404:64541404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200398762
CDS Mutation	c.5303C>T
AA Mutation	p.Ala1768Val(p.A1768V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64633791:64633791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1945T>G
AA Mutation	p.Phe649Val(p.F649V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64561633:64561633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4643A>G
AA Mutation	p.Asp1548Gly(p.D1548G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64651093:64651093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1387G>A
AA Mutation	p.Ala463Thr(p.A463T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64655871:64655871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974C>T
AA Mutation	p.Ala325Val(p.A325V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64686769:64686769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64607062:64607062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3372A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64602190:64602190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3771T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64596869:64596869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4140C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64649703:64649703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1539C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64594291:64594291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201072070
CDS Mutation	c.4323C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64550958:64550958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746991473
CDS Mutation	c.4803G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64596917:64596917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374058008
CDS Mutation	c.4092C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64633762:64633762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754577175
CDS Mutation	c.1974C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64541156:64541156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531081510
CDS Mutation	c.5460G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000498707
Start	64633871:64633871(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1865delA
AA Mutation	p.Asn622MetfsTer7(p.N622Mfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000498707
Start	64546827:64546827(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs754786025
CDS Mutation	c.4995delC
AA Mutation	p.Ser1666ValfsTer7(p.S1666Vfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000498707
Start	64681243:64681243(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.637delC
AA Mutation	p.Gln213ArgfsTer42(p.Q213Rfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000498707
Start	64641922:64641922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1782G>A
AA Mutation	p.Trp594Ter(p.W594*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000498707
Start	64541608:64541609(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5209dupC
AA Mutation	p.Gln1737ProfsTer10(p.Q1737Pfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript