Mutation

Primary Site >> Stomach Cancer

Gene >> AMER1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64191929:64191929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358T>C
AA Mutation	p.Leu453Pro(p.L453P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64191213:64191213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759613339
CDS Mutation	c.2074G>A
AA Mutation	p.Glu692Lys(p.E692K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64192382:64192382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905A>G
AA Mutation	p.Asn302Ser(p.N302S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64191645:64191645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1642T>C
AA Mutation	p.Ser548Pro(p.S548P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64192665:64192665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772338892
CDS Mutation	c.622G>A
AA Mutation	p.Val208Met(p.V208M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64191188:64191188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2099C>A
AA Mutation	p.Pro700His(p.P700H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64193129:64193129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.158A>G
AA Mutation	p.Lys53Arg(p.K53R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64192563:64192563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724A>T
AA Mutation	p.Thr242Ser(p.T242S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64190223:64190223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3064C>T
AA Mutation	p.Arg1022Cys(p.R1022C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64191947:64191947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1340G>T
AA Mutation	p.Gly447Val(p.G447V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64191897:64191897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767567473
CDS Mutation	c.1390G>A
AA Mutation	p.Ala464Thr(p.A464T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000330258
Start	64189952:64189952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3335A>C
AA Mutation	p.Glu1112Ala(p.E1112A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330258
Start	64191901:64191901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1386A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330258
Start	64193146:64193146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187016794
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330258
Start	64190176:64190176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3111G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330258
Start	64190429:64190429(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2858delC
AA Mutation	p.Pro953GlnfsTer23(p.P953Qfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330258
Start	64192837:64192879(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.408_450delTTTGGAGACAGGCTCCAGATGTAAGACATCTGTGGCTGGAGCC
AA Mutation	p.Leu137GlnfsTer19(p.L137Qfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330258
Start	64192768:64192768(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.519delT
AA Mutation	p.Phe173LeufsTer36(p.F173Lfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000330258
Start	64192131:64192131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1156G>T
AA Mutation	p.Glu386Ter(p.E386*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330258
Start	64192243:64192244(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1043dupG
AA Mutation	p.Gln349ProfsTer29(p.Q349Pfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript