Mutation

Primary Site >> Stomach Cancer

Gene >> MYO9B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17205295:17205295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5023C>T
AA Mutation	p.His1675Tyr(p.H1675Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17206259:17206259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5269G>A
AA Mutation	p.Val1757Ile(p.V1757I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17180989:17180989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185142767
CDS Mutation	c.2282G>A
AA Mutation	p.Arg761His(p.R761H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17202205:17202205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767106410
CDS Mutation	c.4738C>T
AA Mutation	p.Arg1580Cys(p.R1580C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17187999:17187999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2642C>T
AA Mutation	p.Thr881Ile(p.T881I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17202223:17202223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4756A>G
AA Mutation	p.Asn1586Asp(p.N1586D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17172445:17172445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1903C>T
AA Mutation	p.His635Tyr(p.H635Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17172762:17172762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1939T>G
AA Mutation	p.Phe647Val(p.F647V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17211960:17211960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377015078
CDS Mutation	c.6124G>A
AA Mutation	p.Ala2042Thr(p.A2042T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17202145:17202145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200430280
CDS Mutation	c.4678G>A
AA Mutation	p.Val1560Met(p.V1560M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17102489:17102489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761009241
CDS Mutation	c.772G>A
AA Mutation	p.Ala258Thr(p.A258T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000594824
Start	17184932:17184932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2441C>T
AA Mutation	p.Ser814Phe(p.S814F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594824
Start	17180978:17180978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2271C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594824
Start	17211722:17211722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568384629
CDS Mutation	c.6006G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594824
Start	17205291:17205291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543470706
CDS Mutation	c.5019C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594824
Start	17197819:17197819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772690679
CDS Mutation	c.4074C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594824
Start	17172941:17172941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2118C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594824
Start	17197816:17197816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368527258
CDS Mutation	c.4071G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594824
Start	17187952:17187952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371481926
CDS Mutation	c.2595C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594824
Start	17102422:17102422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369894348
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594824
Start	17200787:17200787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766726427
CDS Mutation	c.4521C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000594824
Start	17211897:17211897(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6065delC
AA Mutation	p.Pro2022LeufsTer31(p.P2022Lfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000594824
Start	17212009:17212009(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6178delC
AA Mutation	p.Arg2060GlyfsTer68(p.R2060Gfs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000594824
Start	17209698:17209698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5737C>T
AA Mutation	p.Arg1913Ter(p.R1913*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript