Mutation

Primary Site >> Stomach Cancer

Gene >> VEPH1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157286642:157286642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2043A>C
AA Mutation	p.Glu681Asp(p.E681D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000362010
Start	157286559:157286559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2126C>A
AA Mutation	p.Thr709Asn(p.T709N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157470389:157470389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532806977
CDS Mutation	c.279C>G
AA Mutation	p.Asn93Lys(p.N93K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157470451:157470451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751210034
CDS Mutation	c.217G>A
AA Mutation	p.Glu73Lys(p.E73K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157265546:157265546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2245C>A
AA Mutation	p.Leu749Met(p.L749M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157363372:157363372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1727C>A
AA Mutation	p.Thr576Asn(p.T576N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157261230:157261230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2406G>T
AA Mutation	p.Lys802Asn(p.K802N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157363721:157363721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201025388
CDS Mutation	c.1378G>A
AA Mutation	p.Val460Met(p.V460M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157363509:157363509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1590G>T
AA Mutation	p.Gln530His(p.Q530H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157265576:157265576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151166199
CDS Mutation	c.2215C>T
AA Mutation	p.Arg739Cys(p.R739C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157428444:157428444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.574C>A
AA Mutation	p.Gln192Lys(p.Q192K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362010
Start	157470488:157470488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362010
Start	157313720:157313720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1911T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000362010
Start	157363532:157363532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1567G>T
AA Mutation	p.Glu523Ter(p.E523*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000362010
Start	157460338:157460339(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.371dupC
AA Mutation	p.Val125SerfsTer26(p.V125Sfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript