Mutation

Primary Site >> Stomach Cancer

Gene >> INSR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302850
Start	7143031:7143031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377048253
CDS Mutation	c.2327C>T
AA Mutation	p.Thr776Met(p.T776M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302850
Start	7170588:7170588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556950372
CDS Mutation	c.1432C>T
AA Mutation	p.Arg478Cys(p.R478C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302850
Start	7184331:7184331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138528064
CDS Mutation	c.959C>T
AA Mutation	p.Thr320Met(p.T320M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302850
Start	7122761:7122761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767224035
CDS Mutation	c.3382C>T
AA Mutation	p.Arg1128Cys(p.R1128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302850
Start	7166339:7166339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1676T>C
AA Mutation	p.Val559Ala(p.V559A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302850
Start	7132164:7132164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2836G>A
AA Mutation	p.Asp946Asn(p.D946N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302850
Start	7120719:7120719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766867210
CDS Mutation	c.3560C>T
AA Mutation	p.Thr1187Met(p.T1187M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302850
Start	7117105:7117105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4100G>A
AA Mutation	p.Gly1367Asp(p.G1367D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302850
Start	7117204:7117204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4001A>G
AA Mutation	p.His1334Arg(p.H1334R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302850
Start	7117139:7117139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146490822
CDS Mutation	c.4066G>A
AA Mutation	p.Glu1356Lys(p.E1356K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302850
Start	7170567:7170567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1453G>A
AA Mutation	p.Ala485Thr(p.A485T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302850
Start	7170598:7170598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1422A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302850
Start	7132300:7132300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2700C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302850
Start	7152770:7152770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2187G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302850
Start	7117287:7117287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368279043
CDS Mutation	c.3918C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302850
Start	7184567:7184567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302850
Start	7184534:7184534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769511771
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302850
Start	7166161:7166164(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1851_1854delAGAT
AA Mutation	p.Asp618ProfsTer22(p.D618Pfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302850
Start	7117180:7117180(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4025delG
AA Mutation	p.Gly1342AlafsTer23(p.G1342Afs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000302850
Start	7141691:7141691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2668C>T
AA Mutation	p.Arg890Ter(p.R890*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000302850
Start	7167967:7167967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1610+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000302850
Start	7150495:7150495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2267+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript