Mutation

Primary Site >> Stomach Cancer

Gene >> IGF2R

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160024687:160024687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629A>T
AA Mutation	p.Asn210Ile(p.N210I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160062599:160062599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3650G>T
AA Mutation	p.Cys1217Phe(p.C1217F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160064842:160064842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4056G>C
AA Mutation	p.Leu1352Phe(p.L1352F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160040637:160040637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750670588
CDS Mutation	c.1393G>A
AA Mutation	p.Ala465Thr(p.A465T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160080164:160080164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140022962
CDS Mutation	c.5722A>G
AA Mutation	p.Ile1908Val(p.I1908V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160061508:160061508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3268G>A
AA Mutation	p.Ala1090Thr(p.A1090T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160063547:160063547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3803A>T
AA Mutation	p.Asp1268Val(p.D1268V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160058912:160058912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2905G>A
AA Mutation	p.Val969Ile(p.V969I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160032695:160032695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027C>T
AA Mutation	p.Pro343Ser(p.P343S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160045823:160045823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1844C>T
AA Mutation	p.Ala615Val(p.A615V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160069891:160069891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4276G>A
AA Mutation	p.Ala1426Thr(p.A1426T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160102581:160102581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6905G>A
AA Mutation	p.Arg2302Gln(p.R2302Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160073940:160073940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5131G>A
AA Mutation	p.Ala1711Thr(p.A1711T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	159991269:159991269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235C>T
AA Mutation	p.Pro79Ser(p.P79S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160027214:160027214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746024088
CDS Mutation	c.676C>T
AA Mutation	p.Arg226Trp(p.R226W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160061549:160061549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3309G>C
AA Mutation	p.Arg1103Ser(p.R1103S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160073272:160073272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140858283
CDS Mutation	c.4750G>A
AA Mutation	p.Val1584Met(p.V1584M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160047897:160047897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2335G>A
AA Mutation	p.Asp779Asn(p.D779N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160047245:160047245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2138C>T
AA Mutation	p.Thr713Ile(p.T713I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160075968:160075968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758109180
CDS Mutation	c.5288C>T
AA Mutation	p.Ala1763Val(p.A1763V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160071968:160071968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4502C>A
AA Mutation	p.Pro1501His(p.P1501H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000356956
Start	160073862:160073862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747421150
CDS Mutation	c.5053G>A
AA Mutation	p.Asp1685Asn(p.D1685N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356956
Start	160096575:160096575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6792C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356956
Start	160047872:160047872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145047577
CDS Mutation	c.2310C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356956
Start	160080151:160080151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5709T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356956
Start	160072871:160072871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4677C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356956
Start	160045788:160045788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139665293
CDS Mutation	c.1809C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356956
Start	160043172:160043172(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1505delT
AA Mutation	p.Val502GlyfsTer55(p.V502Gfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356956
Start	160064456:160064456(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs760021495
CDS Mutation	c.3949delG
AA Mutation	p.Asp1317ThrfsTer27(p.D1317Tfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356956
Start	160009123:160009123(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.405delG
AA Mutation	p.Thr137ProfsTer8(p.T137Pfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356956
Start	160027223:160027223(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.690delC
AA Mutation	p.Gly231AlafsTer7(p.G231Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000356956
Start	160105013:160105013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7405C>T
AA Mutation	p.Gln2469Ter(p.Q2469*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	inframe_insertion;splice_region_variant
Transcription ID	ENST00000356956
Start	159991185:159991186(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.156_173dupATGGGAAGCTGTTGATAC
AA Mutation	p.Trp53_Thr58dup(p.W53_T58dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript