Mutation

Primary Site >> Stomach Cancer

Gene >> DVL3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184166491:184166491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778117558
CDS Mutation	c.949C>T
AA Mutation	p.Arg317Trp(p.R317W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184167583:184167583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202T>C
AA Mutation	p.Leu401Pro(p.L401P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184167667:184167667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286G>A
AA Mutation	p.Arg429His(p.R429H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184166203:184166203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841A>G
AA Mutation	p.Ile281Val(p.I281V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184170681:184170681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2077G>A
AA Mutation	p.Glu693Lys(p.E693K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184166613:184166613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751639591
CDS Mutation	c.988A>G
AA Mutation	p.Thr330Ala(p.T330A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184170348:184170348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744G>A
AA Mutation	p.Gly582Ser(p.G582S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184164378:184164378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343C>A
AA Mutation	p.Pro115Thr(p.P115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184164846:184164846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514G>A
AA Mutation	p.Gly172Ser(p.G172S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000313143
Start	184165205:184165205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760208714
CDS Mutation	c.692G>A
AA Mutation	p.Arg231Gln(p.R231Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184163677:184163677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143411607
CDS Mutation	c.182C>T
AA Mutation	p.Ser61Leu(p.S61L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184166937:184166937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1160C>A
AA Mutation	p.Thr387Asn(p.T387N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313143
Start	184170623:184170623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372777365
CDS Mutation	c.2019C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313143
Start	184167587:184167587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778878747
CDS Mutation	c.1206C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313143
Start	184170452:184170452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1848G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313143
Start	184166262:184166262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313143
Start	184167944:184167944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201946541
CDS Mutation	c.1377G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313143
Start	184170485:184170485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1881G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313143
Start	184166938:184166938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1161C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313143
Start	184166184:184166184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313143
Start	184170134:184170134(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1631delC
AA Mutation	p.Pro544ArgfsTer124(p.P544Rfs*124)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313143
Start	184164375:184164375(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.344delC
AA Mutation	p.Pro115HisfsTer44(p.P115Hfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript