Mutation

Primary Site >> Stomach Cancer

Gene >> CTNND1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57803763:57803763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1563T>G
AA Mutation	p.Ile521Met(p.I521M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57808245:57808245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2044G>A
AA Mutation	p.Glu682Lys(p.E682K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57805910:57805910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1751G>A
AA Mutation	p.Arg584Gln(p.R584Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57808471:57808471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199570555
CDS Mutation	c.2173C>T
AA Mutation	p.Arg725Trp(p.R725W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57791579:57791579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.101G>A
AA Mutation	p.Arg34Gln(p.R34Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57795607:57795607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298C>A
AA Mutation	p.Pro100Thr(p.P100T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57814325:57814325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369783710
CDS Mutation	c.2653C>T
AA Mutation	p.Arg885Trp(p.R885W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57804695:57804695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552330982
CDS Mutation	c.1637G>A
AA Mutation	p.Arg546Gln(p.R546Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57796859:57796859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.823T>C
AA Mutation	p.Phe275Leu(p.F275L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399050
Start	57803668:57803668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1468G>A
AA Mutation	p.Val490Met(p.V490M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399050
Start	57815464:57815464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372445902
CDS Mutation	c.2772C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399050
Start	57805905:57805905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1746T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399050
Start	57796598:57796598(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.566delG
AA Mutation	p.Gly189AspfsTer46(p.G189Dfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399050
Start	57802117:57802117(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1346delA
AA Mutation	p.Asn449ThrfsTer49(p.N449Tfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399050
Start	57802037:57802037(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1265delA
AA Mutation	p.Lys422ArgfsTer26(p.K422Rfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000399050
Start	57806917:57806917(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1902delA
AA Mutation	p.Lys634AsnfsTer3(p.K634Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
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

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000399050
Start	57808210:57808210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2009C>A
AA Mutation	p.Ser670Ter(p.S670*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
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

ID	20
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

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000399050
Start	57802148:57802148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372C>T
AA Mutation	p.Arg458Ter(p.R458*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000399050
Start	57802106:57802106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330A>T
AA Mutation	p.Lys444Ter(p.K444*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399050
Start	57802116:57802117(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1346dupA
AA Mutation	p.Asn449LysfsTer3(p.N449Kfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399050
Start	57811477:57811478(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2634dupA
AA Mutation	p.Ser879IlefsTer3(p.S879Ifs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000399050
Start	57802179:57802190(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1407_1418delTGAAGTTATTAC
AA Mutation	p.Glu470_Thr473del(p.E470_T473del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript