Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CTNNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41225693:41225693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768T>G
AA Mutation	p.Ile256Met(p.I256M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41239312:41239312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2316T>A
AA Mutation	p.Asn772Lys(p.N772K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
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

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41225167:41225167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.455C>G
AA Mutation	p.Ala152Gly(p.A152G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41235785:41235785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1745G>A
AA Mutation	p.Arg582Gln(p.R582Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233406:41233406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147T>C
AA Mutation	p.Trp383Arg(p.W383R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224577:41224577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.65T>A
AA Mutation	p.Val22Asp(p.V22D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41235742:41235742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702G>A
AA Mutation	p.Glu568Lys(p.E568K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation 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

Mutation ID	10
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

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41225437:41225437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599G>A
AA Mutation	p.Arg200His(p.R200H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
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

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41236401:41236401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1856G>A
AA Mutation	p.Cys619Tyr(p.C619Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41225194:41225194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.482A>T
AA Mutation	p.Asn161Ile(p.N161I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
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

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41227272:41227272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001A>C
AA Mutation	p.Glu334Ala(p.E334A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233539:41233539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196A>C
AA Mutation	p.Glu399Ala(p.E399A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41234158:41234158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1544G>A
AA Mutation	p.Arg515Gln(p.R515Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41225834:41225834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.909T>G
AA Mutation	p.Ile303Met(p.I303M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233689:41233689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346G>A
AA Mutation	p.Arg449His(p.R449H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
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

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41227331:41227331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1060A>C
AA Mutation	p.Lys354Gln(p.K354Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41224981:41224981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269G>A
AA Mutation	p.Arg90Gln(p.R90Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41225800:41225800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875A>C
AA Mutation	p.Lys292Thr(p.K292T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41225692:41225692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767T>C
AA Mutation	p.Ile256Thr(p.I256T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349496
Start	41224997:41224997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.285A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349496
Start	41224637:41224637(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.125delC
AA Mutation	p.Thr42LysfsTer5(p.T42Kfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349496
Start	41225733:41225733(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.811delA
AA Mutation	p.Met271TrpfsTer5(p.M271Wfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349496
Start	41225827:41225831(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.902_906delTTCAA
AA Mutation	p.Leu301HisfsTer16(p.L301Hfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000349496
Start	41224587:41224587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75G>A
AA Mutation	p.Trp25Ter(p.W25*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349496
Start	41225020:41225021(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.308_309insTTATTTAAACTATTATACACTA
AA Mutation	p.Leu103PhefsTer10(p.L103Ffs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000349496
Start	41224643:41224645(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.133_135delTCT
AA Mutation	p.Ser45del(p.S45del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000349496
Start	41224597:41224608(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.88_99delTACCTGGACTCT
AA Mutation	p.Tyr30_Ser33del(p.Y30_S33del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CTNNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41234163:41234163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1549C>T
AA Mutation	p.Leu517Phe(p.L517F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233749:41233749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1406G>A
AA Mutation	p.Arg469His(p.R469H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
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

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41225188:41225188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476T>C
AA Mutation	p.Leu159Pro(p.L159P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233406:41233406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147T>G
AA Mutation	p.Trp383Gly(p.W383G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41234158:41234158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1544G>A
AA Mutation	p.Arg515Gln(p.R515Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000349496
Start	41233764:41233764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1421G>A
AA Mutation	p.Arg474Gln(p.R474Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349496
Start	41224638:41224638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000349496
Start	41225144:41225145(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.435_491dupTGCAGAACTTGCCACACGTGCAATCCCTGAACTGACAAAACTGCTAAATGACGAGGA
AA Mutation	p.Ala146_Asp164dup(p.A146_D164dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript