Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CTNND1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57809370:57809370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2339A>T
AA Mutation	p.Asn780Ile(p.N780I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57809302:57809302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2271G>T
AA Mutation	p.Lys757Asn(p.K757N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57815465:57815465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2773G>A
AA Mutation	p.Asp925Asn(p.D925N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57796827:57796827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.791G>A
AA Mutation	p.Arg264Gln(p.R264Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000399050
Start	57803623:57803623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423A>C
AA Mutation	p.Thr475Pro(p.T475P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57803756:57803756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758420026
CDS Mutation	c.1556G>A
AA Mutation	p.Arg519His(p.R519H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57796688:57796688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.652G>A
AA Mutation	p.Glu218Lys(p.E218K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57801837:57801837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754613241
CDS Mutation	c.1061G>A
AA Mutation	p.Arg354His(p.R354H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57791582:57791582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104G>A
AA Mutation	p.Arg35His(p.R35H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57808523:57808523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201606412
CDS Mutation	c.2225G>A
AA Mutation	p.Arg742His(p.R742H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57796890:57796890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.854A>G
AA Mutation	p.Asp285Gly(p.D285G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57808213:57808213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2012T>G
AA Mutation	p.Leu671Arg(p.L671R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57796781:57796781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Trp(p.R249W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57803666:57803666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1466T>G
AA Mutation	p.Ile489Ser(p.I489S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57796989:57796989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.953T>G
AA Mutation	p.Leu318Arg(p.L318R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57805934:57805934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1775G>A
AA Mutation	p.Arg592Gln(p.R592Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399050
Start	57796594:57796594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399050
Start	57796471:57796471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372514468
CDS Mutation	c.435G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399050
Start	57794072:57794072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399050
Start	57796612:57796612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399050
Start	57802057:57802057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1281A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399050
Start	57810192:57810192(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2523delA
AA Mutation	p.Glu842LysfsTer10(p.E842Kfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000399050
Start	57808531:57808531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2233G>T
AA Mutation	p.Glu745Ter(p.E745*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000399050
Start	57811420:57811420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2572C>T
AA Mutation	p.Arg858Ter(p.R858*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000399050
Start	57803698:57803698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1498G>T
AA Mutation	p.Glu500Ter(p.E500*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000399050
Start	57796814:57796814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778C>T
AA Mutation	p.Gln260Ter(p.Q260*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399050
Start	57809427:57809428(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2397dupA
AA Mutation	p.Gln800ThrfsTer4(p.Q800Tfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399050
Start	57814353:57814354(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2682dupA
AA Mutation	p.Ser895IlefsTer8(p.S895Ifs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000399050
Start	57801731:57801731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CTNND1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57796488:57796488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776232220
CDS Mutation	c.452G>A
AA Mutation	p.Arg151Gln(p.R151Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57801911:57801911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1135T>G
AA Mutation	p.Leu379Val(p.L379V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399050
Start	57801742:57801742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000399050
Start	57810131:57810131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2458C>T
AA Mutation	p.Arg820Ter(p.R820*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000399050
Start	57815447:57815447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2755C>T
AA Mutation	p.Arg919Ter(p.R919*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript