Mutation

Primary Site >> Stomach Cancer

Gene >> DPYSL3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147395678:147395678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1505C>T
AA Mutation	p.Pro502Leu(p.P502L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147408790:147408790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628A>G
AA Mutation	p.Thr210Ala(p.T210A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147395696:147395696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1487G>T
AA Mutation	p.Arg496Met(p.R496M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000398514
Start	147397844:147397844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758085369
CDS Mutation	c.1283C>T
AA Mutation	p.Ala428Val(p.A428V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147401610:147401610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898G>A
AA Mutation	p.Ala300Thr(p.A300T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147399135:147399135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757343684
CDS Mutation	c.1228G>A
AA Mutation	p.Val410Ile(p.V410I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147399234:147399234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754356799
CDS Mutation	c.1129G>A
AA Mutation	p.Glu377Lys(p.E377K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147408736:147408736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682C>A
AA Mutation	p.Pro228Thr(p.P228T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147415807:147415807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380C>T
AA Mutation	p.Ala127Val(p.A127V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147418611:147418611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149T>G
AA Mutation	p.Ile50Ser(p.I50S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147400760:147400760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1042T>G
AA Mutation	p.Phe348Val(p.F348V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398514
Start	147401614:147401614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200777055
CDS Mutation	c.894G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398514
Start	147399136:147399136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779181977
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398514
Start	147400821:147400821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.981G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398514
Start	147408776:147408776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.642A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398514
Start	147395638:147395638(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1545delC
AA Mutation	p.Ala516GlnfsTer15(p.A516Qfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000398514
Start	147405611:147405611(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.810delA
AA Mutation	p.Gly271GlufsTer3(p.G271Efs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398514
Start	147412652:147412652(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.577delG
AA Mutation	p.Ala193ProfsTer25(p.A193Pfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000398514
Start	147408727:147408727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	20
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000398514
Start	147412689:147412689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript