Colon Cancer: Gene >> CTNNA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138924659:138924659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1696G>A
AA Mutation	p.Gly566Arg(p.G566R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138924615:138924615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1652G>T
AA Mutation	p.Arg551Leu(p.R551L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138934079:138934079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2711A>G
AA Mutation	p.Asp904Gly(p.D904G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138783217:138783217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146A>G
AA Mutation	p.Asn49Ser(p.N49S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138827711:138827711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1055T>C
AA Mutation	p.Met352Thr(p.M352T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138824602:138824602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661C>A
AA Mutation	p.Leu221Ile(p.L221I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138934057:138934057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2689C>A
AA Mutation	p.Leu897Ile(p.L897I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138925289:138925289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1781C>T
AA Mutation	p.Ala594Val(p.A594V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138932624:138932624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2345G>A
AA Mutation	p.Arg782His(p.R782H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138827683:138827683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027G>A
AA Mutation	p.Ala343Thr(p.A343T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138924581:138924581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1618C>T
AA Mutation	p.Arg540Cys(p.R540C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138824668:138824668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727C>A
AA Mutation	p.Leu243Met(p.L243M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138904427:138904427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1375G>A
AA Mutation	p.Ala459Thr(p.A459T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138932672:138932672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2393C>T
AA Mutation	p.Ala798Val(p.A798V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138934063:138934063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2695G>A
AA Mutation	p.Glu899Lys(p.E899K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138782022:138782022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98T>C
AA Mutation	p.Val33Ala(p.V33A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138783364:138783364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746832628
CDS Mutation	c.293G>A
AA Mutation	p.Arg98Gln(p.R98Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138886228:138886228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1079G>T
AA Mutation	p.Arg360Ile(p.R360I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138934019:138934019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2651G>A
AA Mutation	p.Arg884Gln(p.R884Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000302763
Start	138812184:138812184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470T>C
AA Mutation	p.Val157Ala(p.V157A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138932676:138932676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2397G>T
AA Mutation	p.Glu799Asp(p.E799D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302763
Start	138824598:138824598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751221688
CDS Mutation	c.657G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302763
Start	138925365:138925365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1857T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302763
Start	138904390:138904390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1338T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302763
Start	138917858:138917858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1506C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302763
Start	138783191:138783191(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.122delA
AA Mutation	p.Asn41ThrfsTer54(p.N41Tfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302763
Start	138812254:138812254(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.543delA
AA Mutation	p.Lys181AsnfsTer7(p.K181Nfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302763
Start	138917827:138917827(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1479delA
AA Mutation	p.Lys493AsnfsTer31(p.K493Nfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302763
Start	138933859:138933862(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2494_2497delACAG
AA Mutation	p.Thr832Ter(p.T832*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000302763
Start	138933945:138933945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2577G>A
AA Mutation	p.Trp859Ter(p.W859*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000302763
Start	138904403:138904403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201498915
CDS Mutation	c.1351C>T
AA Mutation	p.Arg451Ter(p.R451*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000302763
Start	138930894:138930894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2257G>T
AA Mutation	p.Gly753Ter(p.G753*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302763
Start	138810041:138810042(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.308dupT
AA Mutation	p.Leu103PhefsTer12(p.L103Ffs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CTNNA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138933987:138933987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376239375
CDS Mutation	c.2619G>T
AA Mutation	p.Glu873Asp(p.E873D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138924582:138924582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139655691
CDS Mutation	c.1619G>A
AA Mutation	p.Arg540His(p.R540H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302763
Start	138781973:138781973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.49A>C
AA Mutation	p.Ser17Arg(p.S17R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript