Mutation

Primary Site >> Stomach Cancer

Gene >> THSD1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378215:52378215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1755C>G
AA Mutation	p.Phe585Leu(p.F585L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378513:52378513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1457C>T
AA Mutation	p.Thr486Met(p.T486M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378226:52378226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744G>A
AA Mutation	p.Ala582Thr(p.A582T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378529:52378529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762147836
CDS Mutation	c.1441G>A
AA Mutation	p.Gly481Arg(p.G481R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52397240:52397240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1013G>C
AA Mutation	p.Arg338Thr(p.R338T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52398138:52398138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115A>T
AA Mutation	p.Asn39Tyr(p.N39Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52397469:52397469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784C>T
AA Mutation	p.Pro262Ser(p.P262S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52397723:52397723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530A>G
AA Mutation	p.Glu177Gly(p.E177G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378525:52378525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1445G>A
AA Mutation	p.Gly482Glu(p.G482E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378115:52378115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1855A>C
AA Mutation	p.Ser619Arg(p.S619R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52377799:52377799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200635008
CDS Mutation	c.2171C>A
AA Mutation	p.Pro724His(p.P724H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378205:52378205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1765T>A
AA Mutation	p.Ser589Thr(p.S589T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52397451:52397451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201109452
CDS Mutation	c.802G>A
AA Mutation	p.Val268Ile(p.V268I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52397870:52397870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383C>A
AA Mutation	p.Pro128His(p.P128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378262:52378262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1708G>A
AA Mutation	p.Ala570Thr(p.A570T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52397325:52397325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766570615
CDS Mutation	c.928A>G
AA Mutation	p.Met310Val(p.M310V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378688:52378688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282A>G
AA Mutation	p.Ile428Val(p.I428V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378010:52378010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1960G>T
AA Mutation	p.Ala654Ser(p.A654S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52377640:52377640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2330C>A
AA Mutation	p.Pro777His(p.P777H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52386121:52386121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087C>T
AA Mutation	p.Arg363Cys(p.R363C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258613
Start	52398034:52398034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258613
Start	52378602:52378602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1368C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258613
Start	52397632:52397632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258613
Start	52397611:52397612(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.641_642delAT
AA Mutation	p.Tyr214CysfsTer21(p.Y214Cfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258613
Start	52397486:52397487(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.766dupG
AA Mutation	p.Val256GlyfsTer36(p.V256Gfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript