Mutation

Primary Site >> Stomach Cancer

Gene >> GLI2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120989341:120989341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770059172
CDS Mutation	c.3427C>T
AA Mutation	p.Pro1143Ser(p.P1143S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120989669:120989669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3755C>T
AA Mutation	p.Pro1252Leu(p.P1252L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120986444:120986444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2123C>T
AA Mutation	p.Ala708Val(p.A708V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120986503:120986503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2182C>T
AA Mutation	p.Arg728Trp(p.R728W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120984570:120984570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768557650
CDS Mutation	c.1783G>A
AA Mutation	p.Val595Ile(p.V595I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120982863:120982863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1666C>T
AA Mutation	p.Arg556Cys(p.R556C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120978483:120978483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150170739
CDS Mutation	c.1418G>A
AA Mutation	p.Arg473His(p.R473H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120955283:120955283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496C>T
AA Mutation	p.Leu166Phe(p.L166F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120968741:120968741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370333257
CDS Mutation	c.671C>T
AA Mutation	p.Thr224Met(p.T224M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120982846:120982846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1649G>A
AA Mutation	p.Arg550His(p.R550H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120988459:120988459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2545G>A
AA Mutation	p.Ala849Thr(p.A849T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120986296:120986296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777362312
CDS Mutation	c.1975G>A
AA Mutation	p.Gly659Arg(p.G659R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120989770:120989770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3856A>G
AA Mutation	p.Thr1286Ala(p.T1286A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120984585:120984585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113407742
CDS Mutation	c.1798C>T
AA Mutation	p.Arg600Cys(p.R600C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120971990:120971990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1109C>T
AA Mutation	p.Ala370Val(p.A370V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120974966:120974966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1225C>A
AA Mutation	p.Leu409Ile(p.L409I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120989129:120989129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3215C>T
AA Mutation	p.Ala1072Val(p.A1072V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120990191:120990191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4277C>T
AA Mutation	p.Ser1426Leu(p.S1426L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120989055:120989055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749578390
CDS Mutation	c.3141G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120975085:120975085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768259857
CDS Mutation	c.1344C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120990213:120990213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373445921
CDS Mutation	c.4299G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120970528:120970528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369761915
CDS Mutation	c.981G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120990219:120990219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140565050
CDS Mutation	c.4305C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120927416:120927416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120986424:120986424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2103C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120986607:120986607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191591728
CDS Mutation	c.2286G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120955348:120955348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141574408
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120955351:120955351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201287742
CDS Mutation	c.564G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120970564:120970564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120927398:120927398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120978514:120978514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1449C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120990381:120990381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4467C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361492
Start	120951338:120951338(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.355delC
AA Mutation	p.His119ThrfsTer4(p.H119Tfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript