Mutation

Primary Site >> Stomach Cancer

Gene >> HGF

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000222390
Start	81743353:81743353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764746019
CDS Mutation	c.865G>A
AA Mutation	p.Ala289Thr(p.A289T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81717336:81717336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301A>C
AA Mutation	p.Lys434Thr(p.K434T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81745045:81745045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.701G>C
AA Mutation	p.Arg234Pro(p.R234P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81711498:81711498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1427C>T
AA Mutation	p.Thr476Ile(p.T476I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81757271:81757271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400C>T
AA Mutation	p.Arg134Cys(p.R134C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81743436:81743436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768451705
CDS Mutation	c.782G>A
AA Mutation	p.Arg261His(p.R261H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81745079:81745079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.667A>G
AA Mutation	p.Met223Val(p.M223V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81717253:81717253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1384G>A
AA Mutation	p.Asp462Asn(p.D462N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81702732:81702732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2036G>C
AA Mutation	p.Cys679Ser(p.C679S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81706393:81706393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1651C>T
AA Mutation	p.His551Tyr(p.H551Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81729641:81729641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1004A>G
AA Mutation	p.His335Arg(p.H335R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81717306:81717306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1331A>G
AA Mutation	p.Asp444Gly(p.D444G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81717336:81717336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301A>T
AA Mutation	p.Lys434Met(p.K434M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81725988:81725988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1070C>A
AA Mutation	p.Pro357Gln(p.P357Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81705700:81705700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1811G>A
AA Mutation	p.Cys604Tyr(p.C604Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81743406:81743406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812G>A
AA Mutation	p.Cys271Tyr(p.C271Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81743407:81743407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811T>C
AA Mutation	p.Cys271Arg(p.C271R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81762799:81762799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.162T>A
AA Mutation	p.Asp54Glu(p.D54E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000222390
Start	81752212:81752212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776090604
CDS Mutation	c.533G>A
AA Mutation	p.Arg178Gln(p.R178Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222390
Start	81752145:81752145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000222390
Start	81758745:81758745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314C>A
AA Mutation	p.Ser105Ter(p.S105*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000222390
Start	81752204:81752204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541C>T
AA Mutation	p.Arg181Ter(p.R181*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000222390
Start	81743472:81743472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript