Mutation

Primary Site >> Stomach Cancer

Gene >> SND1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	128089654:128089654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2584A>G
AA Mutation	p.Met862Val(p.M862V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	128074547:128074547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752279583
CDS Mutation	c.1825G>A
AA Mutation	p.Gly609Ser(p.G609S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127807505:127807505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174C>T
AA Mutation	p.Pro392Ser(p.P392S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	128092005:128092005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2680C>T
AA Mutation	p.Arg894Cys(p.R894C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127686653:127686653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773076395
CDS Mutation	c.119G>T
AA Mutation	p.Arg40Leu(p.R40L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	128091843:128091843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2629G>A
AA Mutation	p.Glu877Lys(p.E877K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	128081456:128081456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2065G>A
AA Mutation	p.Glu689Lys(p.E689K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127807502:127807502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171C>T
AA Mutation	p.Arg391Cys(p.R391C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000354725
Start	128081501:128081501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148285818
CDS Mutation	c.2110G>A
AA Mutation	p.Gly704Ser(p.G704S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127702501:127702501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656T>C
AA Mutation	p.Val219Ala(p.V219A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127721393:127721393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1145A>G
AA Mutation	p.Asn382Ser(p.N382S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354725
Start	127929259:127929259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138583964
CDS Mutation	c.1599C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354725
Start	127698928:127698928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354725
Start	128089575:128089575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201745504
CDS Mutation	c.2505C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354725
Start	128089617:128089617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771438370
CDS Mutation	c.2547C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354725
Start	128085759:128085759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2283C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354725
Start	127721364:127721364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762720042
CDS Mutation	c.1116C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354725
Start	127807501:127807501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1170G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354725
Start	128084776:128084776(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2168delC
AA Mutation	p.Pro723LeufsTer2(p.P723Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354725
Start	128084799:128084799(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2191delC
AA Mutation	p.Arg731AlafsTer11(p.R731Afs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000354725
Start	127694918:127694918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.319C>T
AA Mutation	p.Arg107Ter(p.R107*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000354725
Start	127721368:127721368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120C>T
AA Mutation	p.Arg374Ter(p.R374*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354725
Start	127686743:127686744(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.212dupA
AA Mutation	p.Asp72GlyfsTer4(p.D72Gfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354725
Start	127807551:127807552(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1226dupA
AA Mutation	p.Leu410AlafsTer14(p.L410Afs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000354725
Start	128085781:128085781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2304+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript