Colon Cancer: Gene >> CTNNA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	67180364:67180364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000G>A
AA Mutation	p.Ala334Thr(p.A334T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	66280588:66280588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1766C>G
AA Mutation	p.Ala589Gly(p.A589G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	66069347:66069347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2120A>G
AA Mutation	p.Asn707Ser(p.N707S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	66766326:66766326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138643733
CDS Mutation	c.1219C>T
AA Mutation	p.Arg407Trp(p.R407W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	66379257:66379257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372758887
CDS Mutation	c.1627C>T
AA Mutation	p.Arg543Trp(p.R543W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	66379242:66379242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1642G>A
AA Mutation	p.Ala548Thr(p.A548T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	67647447:67647447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776250185
CDS Mutation	c.67G>A
AA Mutation	p.Val23Met(p.V23M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	65966626:65966626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2386C>A
AA Mutation	p.Leu796Ile(p.L796I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	66379290:66379290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1594A>G
AA Mutation	p.Asn532Asp(p.N532D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000433211
Start	65966614:65966614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2398G>T
AA Mutation	p.Ala800Ser(p.A800S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	65920554:65920554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2464G>T
AA Mutation	p.Val822Leu(p.V822L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	67606923:67606923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.226A>G
AA Mutation	p.Ile76Val(p.I76V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	67180414:67180414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.950C>T
AA Mutation	p.Ser317Phe(p.S317F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	67521944:67521944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477G>T
AA Mutation	p.Glu159Asp(p.E159D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	67521900:67521900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521A>G
AA Mutation	p.Tyr174Cys(p.Y174C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	65988711:65988711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2246C>T
AA Mutation	p.Ala749Val(p.A749V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	67219657:67219657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793C>A
AA Mutation	p.Pro265Thr(p.P265T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	66766304:66766304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1241A>G
AA Mutation	p.Tyr414Cys(p.Y414C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433211
Start	66280515:66280515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1839C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433211
Start	66775465:66775465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433211
Start	66775483:66775483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1089A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433211
Start	67219697:67219697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000433211
Start	66775513:66775513(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1059delA
AA Mutation	p.Glu354LysfsTer6(p.E354Kfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000433211
Start	65920450:65920450(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2568delA
AA Mutation	p.Lys856AsnfsTer3(p.K856Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000433211
Start	67180475:67180475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771161312
CDS Mutation	c.889C>T
AA Mutation	p.Arg297Ter(p.R297*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000433211
Start	65920449:65920450(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs759618368
CDS Mutation	c.2568dupA
AA Mutation	p.Pro857ThrfsTer4(p.P857Tfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000433211
Start	67180316:67180316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1047+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CTNNA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	65920387:65920387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2631G>T
AA Mutation	p.Lys877Asn(p.K877N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000433211
Start	67606865:67606865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779423519
CDS Mutation	c.284G>A
AA Mutation	p.Arg95His(p.R95H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433211
Start	65988752:65988752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745959148
CDS Mutation	c.2205G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433211
Start	66379234:66379234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773885927
CDS Mutation	c.1650C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433211
Start	67180404:67180404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.960G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433211
Start	65988752:65988752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2205G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000433211
Start	66766308:66766308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237G>T
AA Mutation	p.Glu413Ter(p.E413*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000433211
Start	65920449:65920450(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs759618368
CDS Mutation	c.2568dupA
AA Mutation	p.Pro857ThrfsTer4(p.P857Tfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript