Mutation

Primary Site >> Stomach Cancer

Gene >> CCDC178

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000383096
Start	33092908:33092908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2241A>T
AA Mutation	p.Lys747Asn(p.K747N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	33266925:33266925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760077046
CDS Mutation	c.1400C>A
AA Mutation	p.Thr467Asn(p.T467N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	33224864:33224864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1729G>A
AA Mutation	p.Ala577Thr(p.A577T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	33346327:33346327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779422806
CDS Mutation	c.542G>A
AA Mutation	p.Arg181Gln(p.R181Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	33346404:33346404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465G>C
AA Mutation	p.Lys155Asn(p.K155N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	33212052:33212052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2082C>A
AA Mutation	p.Asn694Lys(p.N694K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	32974626:32974626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2444T>C
AA Mutation	p.Val815Ala(p.V815A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000383096
Start	33267051:33267051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274A>C
AA Mutation	p.Lys425Thr(p.K425T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	33370169:33370169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.229T>G
AA Mutation	p.Phe77Val(p.F77V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	33267286:33267286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1188G>T
AA Mutation	p.Leu396Phe(p.L396F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	33333359:33333359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694C>A
AA Mutation	p.Gln232Lys(p.Q232K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	33266948:33266948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377T>A
AA Mutation	p.Asp459Glu(p.D459E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	33370162:33370162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236A>G
AA Mutation	p.Tyr79Cys(p.Y79C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000383096
Start	33223143:33223143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1895A>G
AA Mutation	p.Lys632Arg(p.K632R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383096
Start	33348966:33348966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383096
Start	32974604:32974604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2466G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383096
Start	33267223:33267223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1251A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383096
Start	33223143:33223143(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1895delA
AA Mutation	p.Lys632ArgfsTer9(p.K632Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383096
Start	33293184:33293184(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749875431
CDS Mutation	c.1151delA
AA Mutation	p.Asn384MetfsTer13(p.N384Mfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383096
Start	33333179:33333179(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769009032
CDS Mutation	c.874delA
AA Mutation	p.Met292TrpfsTer3(p.M292Wfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383096
Start	33333179:33333180(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.873_874delAA
AA Mutation	p.Lys291AsnfsTer11(p.K291Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383096
Start	33267046:33267046(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776882105
CDS Mutation	c.1279delA
AA Mutation	p.Thr427HisfsTer23(p.T427Hfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383096
Start	33346305:33346306(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.563dupT
AA Mutation	p.Leu188PhefsTer12(p.L188Ffs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383096
Start	33224930:33224931(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs765706382
CDS Mutation	c.1662dupA
AA Mutation	p.Leu555ThrfsTer11(p.L555Tfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383096
Start	33211979:33211980(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2154dupA
AA Mutation	p.Asp719ArgfsTer3(p.D719Rfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383096
Start	33226831:33226832(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1617dupA
AA Mutation	p.Leu540ThrfsTer5(p.L540Tfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000383096
Start	33092760:33092760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2388+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	28
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000383096
Start	33212056:33212056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2079-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript