Mutation

Primary Site >> Liver Cancer

Gene >> GLI2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120989501:120989501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3587G>A
AA Mutation	p.Gly1196Glu(p.G1196E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120988307:120988307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2393T>C
AA Mutation	p.Met798Thr(p.M798T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120989905:120989905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3991T>A
AA Mutation	p.Ser1331Thr(p.S1331T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361492
Start	120982717:120982717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1520T>C
AA Mutation	p.Phe507Ser(p.F507S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120797353:120797353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33G>T
AA Mutation	p.Glu11Asp(p.E11D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120990271:120990271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4357A>T
AA Mutation	p.Met1453Leu(p.M1453L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120968791:120968791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768192957
CDS Mutation	c.721G>A
AA Mutation	p.Ala241Thr(p.A241T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120968734:120968734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Trp(p.R222W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120988246:120988246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2332G>A
AA Mutation	p.Gly778Arg(p.G778R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120990434:120990434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4520C>A
AA Mutation	p.Ala1507Asp(p.A1507D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120970523:120970523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976C>A
AA Mutation	p.Gln326Lys(p.Q326K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120990188:120990188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4274G>T
AA Mutation	p.Gly1425Val(p.G1425V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361492
Start	120978500:120978500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121917708
CDS Mutation	c.1435C>T
AA Mutation	p.Arg479Trp(p.R479W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120970522:120970522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.975C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361492
Start	120986388:120986388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2067G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000361492
Start	120988570:120988570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2656C>T
AA Mutation	p.Gln886Ter(p.Q886*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript