Mutation

Primary Site >> Stomach Cancer

Gene >> ADAMTS8

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130408570:130408570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776551880
CDS Mutation	c.1993G>A
AA Mutation	p.Gly665Ser(p.G665S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130419223:130419223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790A>G
AA Mutation	p.Asn264Asp(p.N264D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130414727:130414727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1370G>T
AA Mutation	p.Gly457Val(p.G457V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130405662:130405662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2566A>T
AA Mutation	p.Thr856Ser(p.T856S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130411549:130411549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757519748
CDS Mutation	c.1618C>T
AA Mutation	p.Arg540Trp(p.R540W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130408542:130408542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749722171
CDS Mutation	c.2021G>A
AA Mutation	p.Arg674Gln(p.R674Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130419100:130419100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528234968
CDS Mutation	c.913G>A
AA Mutation	p.Asp305Asn(p.D305N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130408495:130408495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2068A>G
AA Mutation	p.Arg690Gly(p.R690G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130417012:130417012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1024G>A
AA Mutation	p.Asp342Asn(p.D342N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130408833:130408833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34821407
CDS Mutation	c.1858C>T
AA Mutation	p.Arg620Trp(p.R620W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130408473:130408473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2090C>T
AA Mutation	p.Thr697Ile(p.T697I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130411597:130411597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371697073
CDS Mutation	c.1570G>A
AA Mutation	p.Val524Met(p.V524M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000257359
Start	130408819:130408819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1872G>T
AA Mutation	p.Lys624Asn(p.K624N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257359
Start	130427684:130427684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257359
Start	130408499:130408499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2064C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257359
Start	130408798:130408798(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1893delG
AA Mutation	p.Arg632GlyfsTer11(p.R632Gfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript