Mutation

Primary Site >> Stomach Cancer

Gene >> CTNNB1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41238067:41238067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2128C>T
AA Mutation	p.Arg710Cys(p.R710C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
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	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000349496
Start	41225335:41225335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497T>G
AA Mutation	p.Val166Gly(p.V166G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41235800:41235800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1760G>A
AA Mutation	p.Arg587Gln(p.R587Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233734:41233734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1391C>T
AA Mutation	p.Ala464Val(p.A464V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41234218:41234218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1604G>A
AA Mutation	p.Arg535Gln(p.R535Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41227251:41227251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980T>C
AA Mutation	p.Ile327Thr(p.I327T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41236409:41236409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1864G>C
AA Mutation	p.Ala622Pro(p.A622P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41235763:41235763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs797044875
CDS Mutation	c.1723G>A
AA Mutation	p.Gly575Arg(p.G575R)
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>C
AA Mutation	p.Asp32His(p.D32H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
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	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224075:41224075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7A>G
AA Mutation	p.Thr3Ala(p.T3A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
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	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224962:41224962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250G>A
AA Mutation	p.Gly84Arg(p.G84R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41225081:41225081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758551763
CDS Mutation	c.369G>T
AA Mutation	p.Gln123His(p.Q123H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
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	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41225163:41225163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451C>T
AA Mutation	p.Arg151Cys(p.R151C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
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	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233722:41233722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1379T>C
AA Mutation	p.Ile460Thr(p.I460T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41227287:41227287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016C>A
AA Mutation	p.Thr339Asn(p.T339N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41236591:41236591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1958C>A
AA Mutation	p.Thr653Lys(p.T653K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
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	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349496
Start	41225108:41225108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778138109
CDS Mutation	c.396G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349496
Start	41225180:41225180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745411917
CDS Mutation	c.468G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349496
Start	41225777:41225777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773586998
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349496
Start	41233597:41233597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349496
Start	41233713:41233713(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1372delG
AA Mutation	p.Glu458LysfsTer14(p.E458Kfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349496
Start	41225163:41225163(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.451delC
AA Mutation	p.Arg151ValfsTer6(p.R151Vfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349496
Start	41225165:41225169(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.454_458delGCAAT
AA Mutation	p.Ala152ProfsTer2(p.A152Pfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349496
Start	41233689:41233689(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1346delG
AA Mutation	p.Arg449LeufsTer23(p.R449Lfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349496
Start	41227272:41227272(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1005delA
AA Mutation	p.Lys335AsnfsTer10(p.K335Nfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000349496
Start	41233763:41233763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1420C>T
AA Mutation	p.Arg474Ter(p.R474*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000349496
Start	41224995:41224995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283C>T
AA Mutation	p.Arg95Ter(p.R95*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000349496
Start	41224632:41224652(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.121_141delACCACAGCTCCTTCTCTGAGT
AA Mutation	p.Thr41_Ser47del(p.T41_S47del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript