Mutation

Primary Site >> Stomach Cancer

Gene >> SMG1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18817397:18817397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9968A>G
AA Mutation	p.Asp3323Gly(p.D3323G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18863786:18863786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3559G>A
AA Mutation	p.Gly1187Arg(p.G1187R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18849243:18849243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5597C>T
AA Mutation	p.Ser1866Leu(p.S1866L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18853816:18853816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4535G>A
AA Mutation	p.Cys1512Tyr(p.C1512Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18830331:18830331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8831G>T
AA Mutation	p.Arg2944Ile(p.R2944I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18845538:18845538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6110A>G
AA Mutation	p.Glu2037Gly(p.E2037G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18870667:18870667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2435G>A
AA Mutation	p.Arg812His(p.R812H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18815498:18815498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759196617
CDS Mutation	c.10456G>A
AA Mutation	p.Val3486Ile(p.V3486I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18847543:18847543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5906T>G
AA Mutation	p.Val1969Gly(p.V1969G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18863774:18863774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3571T>C
AA Mutation	p.Cys1191Arg(p.C1191R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18833148:18833148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540679816
CDS Mutation	c.8584C>T
AA Mutation	p.Arg2862Trp(p.R2862W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18842421:18842421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6253C>T
AA Mutation	p.Arg2085Cys(p.R2085C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18835043:18835043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776873619
CDS Mutation	c.8179C>T
AA Mutation	p.Arg2727Cys(p.R2727C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18868533:18868533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3020C>T
AA Mutation	p.Ser1007Leu(p.S1007L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18869229:18869229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369378228
CDS Mutation	c.2708G>A
AA Mutation	p.Arg903His(p.R903H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18816325:18816325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10279C>T
AA Mutation	p.His3427Tyr(p.H3427Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000446231
Start	18833058:18833058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8674G>C
AA Mutation	p.Glu2892Gln(p.E2892Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446231
Start	18838125:18838125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7302T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446231
Start	18836156:18836156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7834T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446231
Start	18885601:18885601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446231
Start	18845456:18845456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6192T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446231
Start	18872511:18872511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2004G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446231
Start	18841754:18841754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6507C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446231
Start	18877227:18877227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1524T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446231
Start	18845485:18845485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6163C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446231
Start	18847948:18847948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5709T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446231
Start	18852106:18852106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5013T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446231
Start	18836142:18836142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7848C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000446231
Start	18833121:18833121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8611C>T
AA Mutation	p.Arg2871Ter(p.R2871*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000446231
Start	18847511:18847511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5938C>T
AA Mutation	p.Arg1980Ter(p.R1980*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000446231
Start	18869198:18869198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2739G>A
AA Mutation	p.Trp913Ter(p.W913*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript