Mutation

Primary Site >> Stomach Cancer

Gene >> AMER2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171105:25171105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515G>A
AA Mutation	p.Arg172His(p.R172H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171327:25171327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773634447
CDS Mutation	c.293C>T
AA Mutation	p.Thr98Met(p.T98M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25170434:25170434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186T>C
AA Mutation	p.Cys396Arg(p.C396R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171456:25171456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164C>A
AA Mutation	p.Ala55Asp(p.A55D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171543:25171543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.77G>A
AA Mutation	p.Cys26Tyr(p.C26Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171525:25171525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95C>T
AA Mutation	p.Ala32Val(p.A32V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171019:25171019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.601A>G
AA Mutation	p.Met201Val(p.M201V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171573:25171573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>T
AA Mutation	p.Arg16Leu(p.R16L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25170004:25170004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1616G>C
AA Mutation	p.Ser539Thr(p.S539T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25170898:25170898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553783283
CDS Mutation	c.722C>T
AA Mutation	p.Thr241Met(p.T241M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171249:25171249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25169981:25169981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755445946
CDS Mutation	c.1639C>T
AA Mutation	p.Arg547Trp(p.R547W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25169873:25169873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1747C>T
AA Mutation	p.Arg583Trp(p.R583W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171330:25171330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.290C>T
AA Mutation	p.Pro97Leu(p.P97L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25169841:25169841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1779C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25169682:25169682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1938C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25171221:25171221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25171176:25171176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25171101:25171101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25171452:25171452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000515384
Start	25169952:25169953(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1667_1668delAT
AA Mutation	p.Tyr556Ter(p.Y556*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000515384
Start	25169981:25169981(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1639delC
AA Mutation	p.Arg547GlyfsTer38(p.R547Gfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000515384
Start	25170945:25170967(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.653_675delGCGCGCCCGGGGGCGGCTTGATC
AA Mutation	p.Arg218ProfsTer37(p.R218Pfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript