Mutation

Primary Site >> Stomach Cancer

Gene >> EDNRB

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77918516:77918516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762469442
CDS Mutation	c.58G>A
AA Mutation	p.Gly20Ser(p.G20S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77903293:77903293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664A>C
AA Mutation	p.Ile222Leu(p.I222L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77918536:77918536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38T>G
AA Mutation	p.Val13Gly(p.V13G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77903250:77903250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707A>C
AA Mutation	p.Glu236Ala(p.E236A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77900560:77900560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1046T>G
AA Mutation	p.Leu349Arg(p.L349R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77903567:77903567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524A>C
AA Mutation	p.Lys175Thr(p.K175T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77918533:77918533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41C>T
AA Mutation	p.Ala14Val(p.A14V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77901111:77901111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.898A>T
AA Mutation	p.Met300Leu(p.M300L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77901135:77901135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874T>C
AA Mutation	p.Phe292Leu(p.F292L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77918305:77918305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269G>A
AA Mutation	p.Cys90Tyr(p.C90Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77903520:77903520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571A>T
AA Mutation	p.Ser191Cys(p.S191C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77918549:77918549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25G>A
AA Mutation	p.Gly9Arg(p.G9R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77918336:77918336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238T>C
AA Mutation	p.Ser80Pro(p.S80P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77903290:77903290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751199972
CDS Mutation	c.667G>T
AA Mutation	p.Val223Phe(p.V223F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77903243:77903243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714A>G
AA Mutation	p.Ile238Met(p.I238M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77918558:77918558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16A>G
AA Mutation	p.Ser6Gly(p.S6G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77903175:77903175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.782A>C
AA Mutation	p.Gln261Pro(p.Q261P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000334286
Start	77903505:77903505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586A>C
AA Mutation	p.Ser196Arg(p.S196R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334286
Start	77898296:77898296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334286
Start	77903276:77903276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334286
Start	77918103:77918103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334286
Start	77918379:77918379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200037615
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334286
Start	77918565:77918565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201820859
CDS Mutation	c.9G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334286
Start	77901132:77901132(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769735757
CDS Mutation	c.877delT
AA Mutation	p.Tyr293IlefsTer3(p.Y293Ifs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334286
Start	77899869:77899869(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1184delA
AA Mutation	p.Asn395ThrfsTer27(p.N395Tfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334286
Start	77898296:77898296(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1233delA
AA Mutation	p.Lys411AsnfsTer11(p.K411Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000334286
Start	77901130:77901130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879T>G
AA Mutation	p.Tyr293Ter(p.Y293*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334286
Start	77901131:77901132(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.877dupT
AA Mutation	p.Tyr293LeufsTer7(p.Y293Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript