Mutation

Primary Site >> Stomach Cancer

Gene >> AOC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150857756:150857756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200294204
CDS Mutation	c.1286G>A
AA Mutation	p.Arg429Gln(p.R429Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150857575:150857575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105A>G
AA Mutation	p.Thr369Ala(p.T369A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150857632:150857632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756815729
CDS Mutation	c.1162G>A
AA Mutation	p.Gly388Ser(p.G388S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150857731:150857731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1261A>G
AA Mutation	p.Met421Val(p.M421V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150858846:150858846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1654C>T
AA Mutation	p.Pro552Ser(p.P552S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150857600:150857600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130G>A
AA Mutation	p.Gly377Asp(p.G377D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150857941:150857941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1471A>G
AA Mutation	p.Thr491Ala(p.T491A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150860962:150860962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368330728
CDS Mutation	c.2009C>T
AA Mutation	p.Thr670Met(p.T670M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150860559:150860559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1915C>T
AA Mutation	p.His639Tyr(p.H639Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150856975:150856975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764404660
CDS Mutation	c.505A>G
AA Mutation	p.Thr169Ala(p.T169A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150856768:150856768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577618065
CDS Mutation	c.298G>A
AA Mutation	p.Val100Ile(p.V100I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360937
Start	150857928:150857928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752546192
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360937
Start	150857631:150857631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751075124
CDS Mutation	c.1161C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360937
Start	150857646:150857646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748358249
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360937
Start	150857033:150857033(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.568delC
AA Mutation	p.Arg190GlyfsTer18(p.R190Gfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360937
Start	150861171:150861171(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2222delC
AA Mutation	p.Pro741LeufsTer54(p.P741Lfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360937
Start	150857942:150857942(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1476delC
AA Mutation	p.Glu493ArgfsTer13(p.E493Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360937
Start	150860504:150860504(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1864delC
AA Mutation	p.Leu622TrpfsTer3(p.L622Wfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360937
Start	150856940:150856947(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.475_482delACCAAGCC
AA Mutation	p.Thr159ProfsTer18(p.T159Pfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript