Mutation

Primary Site >> Liver Cancer

Gene >> CTNNB1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224646:41224646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913409
CDS Mutation	c.134C>T
AA Mutation	p.Ser45Phe(p.S45F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224607:41224607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913396
CDS Mutation	c.95A>T
AA Mutation	p.Asp32Val(p.D32V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224622:41224622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913403
CDS Mutation	c.110C>T
AA Mutation	p.Ser37Phe(p.S37F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224633:41224633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913412
CDS Mutation	c.121A>G
AA Mutation	p.Thr41Ala(p.T41A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41227275:41227275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004A>T
AA Mutation	p.Lys335Ile(p.K335I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224607:41224607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913396
CDS Mutation	c.95A>G
AA Mutation	p.Asp32Gly(p.D32G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224619:41224619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107A>C
AA Mutation	p.His36Pro(p.H36P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224622:41224622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913403
CDS Mutation	c.110C>A
AA Mutation	p.Ser37Tyr(p.S37Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224645:41224645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913407
CDS Mutation	c.133T>C
AA Mutation	p.Ser45Pro(p.S45P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224606:41224606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28931588
CDS Mutation	c.94G>A
AA Mutation	p.Asp32Asn(p.D32N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224609:41224609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97T>C
AA Mutation	p.Ser33Pro(p.S33P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224609:41224609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97T>G
AA Mutation	p.Ser33Ala(p.S33A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224616:41224616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104T>G
AA Mutation	p.Ile35Ser(p.I35S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224610:41224610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913400
CDS Mutation	c.98C>T
AA Mutation	p.Ser33Phe(p.S33F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224606:41224606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28931588
CDS Mutation	c.94G>T
AA Mutation	p.Asp32Tyr(p.D32Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224610:41224610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913400
CDS Mutation	c.98C>A
AA Mutation	p.Ser33Tyr(p.S33Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224610:41224610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913400
CDS Mutation	c.98C>G
AA Mutation	p.Ser33Cys(p.S33C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233362:41233362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103T>A
AA Mutation	p.Leu368His(p.L368H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41227275:41227275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004A>C
AA Mutation	p.Lys335Thr(p.K335T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233420:41233420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1161T>A
AA Mutation	p.Asn387Lys(p.N387K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41225391:41225391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553A>G
AA Mutation	p.Arg185Gly(p.R185G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233419:41233419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160A>T
AA Mutation	p.Asn387Ile(p.N387I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224634:41224634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913413
CDS Mutation	c.122C>T
AA Mutation	p.Thr41Ile(p.T41I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224612:41224612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913399
CDS Mutation	c.100G>A
AA Mutation	p.Gly34Arg(p.G34R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224613:41224613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28931589
CDS Mutation	c.101G>T
AA Mutation	p.Gly34Val(p.G34V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224612:41224612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100G>C
AA Mutation	p.Gly34Arg(p.G34R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224646:41224646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913409
CDS Mutation	c.134C>A
AA Mutation	p.Ser45Tyr(p.S45Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233556:41233556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1213C>T
AA Mutation	p.Leu405Phe(p.L405F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224622:41224622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913403
CDS Mutation	c.110C>G
AA Mutation	p.Ser37Cys(p.S37C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233420:41233420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1161T>G
AA Mutation	p.Asn387Lys(p.N387K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233408:41233408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149G>C
AA Mutation	p.Trp383Cys(p.W383C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224621:41224621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913228
CDS Mutation	c.109T>G
AA Mutation	p.Ser37Ala(p.S37A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41227269:41227269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998A>T
AA Mutation	p.Tyr333Phe(p.Y333F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224613:41224613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28931589
CDS Mutation	c.101G>A
AA Mutation	p.Gly34Glu(p.G34E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233418:41233418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159A>T
AA Mutation	p.Asn387Tyr(p.N387Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349496
Start	41233594:41233594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1251C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349496
Start	41233597:41233601(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1255_1259delTGTGC
AA Mutation	p.Cys419SerfsTer6(p.C419Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000349496
Start	41224636:41224659(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.124_147delACAGCTCCTTCTCTGAGTGGTAAA
AA Mutation	p.Thr42_Lys49del(p.T42_K49del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

ID	39
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000349496
Start	41224602:41224616(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.92_106delTGGACTCTGGAATCC
AA Mutation	p.Leu31_Ile35del(p.L31_I35del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

ID	40
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000349496
Start	41224613:41224614(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.101_102insGATTAACTATCAAGATGATGCAGAACTTGCCACACGTGC
AA Mutation	p.Ile35_His36insAsnTyrGlnAspAspAlaGluLeuAlaThrArgAlaIle(p.I35_H36insNYQDDAELATRAI)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript