Mutation

Primary Site >> Stomach Cancer

Gene >> IGF1R

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98957093:98957093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3755A>G
AA Mutation	p.Asn1252Ser(p.N1252S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98707609:98707609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138973619
CDS Mutation	c.142C>T
AA Mutation	p.Arg48Cys(p.R48C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98707960:98707960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493T>A
AA Mutation	p.Ser165Thr(p.S165T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98913267:98913267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1813C>T
AA Mutation	p.Arg605Cys(p.R605C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98707955:98707955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182472366
CDS Mutation	c.488C>T
AA Mutation	p.Ala163Val(p.A163V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98916818:98916818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2143G>A
AA Mutation	p.Glu715Lys(p.E715K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98708018:98708018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551G>T
AA Mutation	p.Gly184Val(p.G184V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98913189:98913189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138992740
CDS Mutation	c.1735G>A
AA Mutation	p.Val579Ile(p.V579I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98934865:98934865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2998A>G
AA Mutation	p.Thr1000Ala(p.T1000A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98891360:98891360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752189789
CDS Mutation	c.676G>A
AA Mutation	p.Glu226Lys(p.E226K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98707733:98707733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266G>A
AA Mutation	p.Arg89Gln(p.R89Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98934874:98934874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3007C>T
AA Mutation	p.Arg1003Trp(p.R1003W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98649633:98649633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52T>A
AA Mutation	p.Phe18Ile(p.F18I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98922326:98922326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753047347
CDS Mutation	c.2380C>T
AA Mutation	p.Arg794Trp(p.R794W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98957203:98957203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3865G>A
AA Mutation	p.Glu1289Lys(p.E1289K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98924556:98924556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2654A>G
AA Mutation	p.Tyr885Cys(p.Y885C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98707913:98707913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446T>A
AA Mutation	p.Leu149His(p.L149H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98942994:98942994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3529C>T
AA Mutation	p.Arg1177Cys(p.R1177C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98957321:98957321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3983G>A
AA Mutation	p.Gly1328Asp(p.G1328D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98899565:98899565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771031733
CDS Mutation	c.1191C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98948670:98948670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758048090
CDS Mutation	c.3684C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98957247:98957247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3909C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98891479:98891479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565401892
CDS Mutation	c.795G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98908883:98908883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537098180
CDS Mutation	c.1446C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98924647:98924647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757589571
CDS Mutation	c.2745G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98707827:98707827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98942936:98942936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28664854
CDS Mutation	c.3471G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98943044:98943044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777500976
CDS Mutation	c.3579G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98957388:98957388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771019606
CDS Mutation	c.4050C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98939356:98939356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375579623
CDS Mutation	c.3453C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98891416:98891416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765728831
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98922223:98922223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754252753
CDS Mutation	c.2277C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98707785:98707785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98899529:98899529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369896687
CDS Mutation	c.1155G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98942985:98942985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3520C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98891353:98891353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268035
Start	98957389:98957389(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4055delG
AA Mutation	p.Gly1352AlafsTer27(p.G1352Afs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268035
Start	98957247:98957247(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3913delC
AA Mutation	p.Leu1305TrpfsTer45(p.L1305Wfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268035
Start	98924626:98924627(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2732_2733dupCT
AA Mutation	p.Gly912LeufsTer26(p.G912Lfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript