Mutation

Primary Site >> Stomach Cancer

Gene >> LATS2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20989277:20989277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503C>T
AA Mutation	p.Thr168Met(p.T168M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20989152:20989152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628C>T
AA Mutation	p.Pro210Ser(p.P210S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20983277:20983277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2429T>C
AA Mutation	p.Phe810Ser(p.F810S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20975298:20975298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2839C>A
AA Mutation	p.Leu947Ile(p.L947I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20988167:20988167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1613C>T
AA Mutation	p.Ala538Val(p.A538V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20988854:20988854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926C>T
AA Mutation	p.Ala309Val(p.A309V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20988591:20988591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1189C>T
AA Mutation	p.Arg397Trp(p.R397W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20983520:20983520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2186T>C
AA Mutation	p.Val729Ala(p.V729A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20981637:20981637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2494A>G
AA Mutation	p.Arg832Gly(p.R832G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20988606:20988606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778627422
CDS Mutation	c.1174G>A
AA Mutation	p.Ala392Thr(p.A392T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20988789:20988789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991C>A
AA Mutation	p.Leu331Met(p.L331M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20989029:20989029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766080720
CDS Mutation	c.751G>A
AA Mutation	p.Ala251Thr(p.A251T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20983532:20983532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775247544
CDS Mutation	c.2174A>G
AA Mutation	p.Asn725Ser(p.N725S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20991296:20991296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451C>T
AA Mutation	p.Arg151Trp(p.R151W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20981549:20981549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562406125
CDS Mutation	c.2582C>T
AA Mutation	p.Ala861Val(p.A861V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20988022:20988022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202224882
CDS Mutation	c.1758C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20988256:20988256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1524C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20988616:20988616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1164G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20975059:20975059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769023154
CDS Mutation	c.3078C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20975092:20975092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762984472
CDS Mutation	c.3045C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20983231:20983231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2475C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20983633:20983633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775335330
CDS Mutation	c.2073C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20988169:20988169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748401705
CDS Mutation	c.1611C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382592
Start	20981577:20981577(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2554delG
AA Mutation	p.Asp852ThrfsTer3(p.D852Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382592
Start	20979722:20979722(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2741delT
AA Mutation	p.Leu914TrpfsTer10(p.L914Wfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382592
Start	20989210:20989210(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.570delC
AA Mutation	p.Tyr191ThrfsTer49(p.Y191Tfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript