Mutation

Primary Site >> Liver Cancer

Gene >> FLNB

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295956
Start	58008829:58008829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755518501
CDS Mutation	c.265C>G
AA Mutation	p.Arg89Gly(p.R89G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295956
Start	58121367:58121367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2990C>G
AA Mutation	p.Thr997Arg(p.T997R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295956
Start	58098786:58098786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1223A>G
AA Mutation	p.Asp408Gly(p.D408G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295956
Start	58135997:58135997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4690A>C
AA Mutation	p.Lys1564Gln(p.K1564Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295956
Start	58109633:58109633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2257G>C
AA Mutation	p.Glu753Gln(p.E753Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295956
Start	58130810:58130810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4292T>A
AA Mutation	p.Leu1431Gln(p.L1431Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295956
Start	58126625:58126625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4085G>T
AA Mutation	p.Gly1362Val(p.G1362V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295956
Start	58008644:58008644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760976111
CDS Mutation	c.80A>G
AA Mutation	p.Asn27Ser(p.N27S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295956
Start	58081664:58081664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295956
Start	58103964:58103964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1489C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000295956
Start	58155967:58155967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6780C>G
AA Mutation	p.Tyr2260Ter(p.Y2260*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript