Mutation

Primary Site >> Stomach Cancer

Gene >> CCDC88A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55346317:55346317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769621745
CDS Mutation	c.899C>T
AA Mutation	p.Ser300Leu(p.S300L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55318976:55318976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3191C>T
AA Mutation	p.Ala1064Val(p.A1064V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55334224:55334224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2597A>G
AA Mutation	p.Asn866Ser(p.N866S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55334765:55334765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2056A>G
AA Mutation	p.Thr686Ala(p.T686A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55388818:55388818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233A>G
AA Mutation	p.Asn78Ser(p.N78S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55295930:55295930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5218C>T
AA Mutation	p.Pro1740Ser(p.P1740S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55328311:55328311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745518858
CDS Mutation	c.2980C>T
AA Mutation	p.Arg994Cys(p.R994C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55362349:55362349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772956921
CDS Mutation	c.586C>T
AA Mutation	p.His196Tyr(p.H196Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55334177:55334177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2644C>T
AA Mutation	p.Arg882Cys(p.R882C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55362439:55362439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496A>G
AA Mutation	p.Asn166Asp(p.N166D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55322538:55322538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3152T>C
AA Mutation	p.Val1051Ala(p.V1051A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55299892:55299892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4772G>C
AA Mutation	p.Gly1591Ala(p.G1591A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55346293:55346293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923A>G
AA Mutation	p.Tyr308Cys(p.Y308C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000436346
Start	55296344:55296344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5005C>T
AA Mutation	p.His1669Tyr(p.H1669Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436346
Start	55317721:55317721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3445C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436346
Start	55334112:55334112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2709G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436346
Start	55308837:55308837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4359C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436346
Start	55334976:55334976(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1845delA
AA Mutation	p.Glu616AsnfsTer33(p.E616Nfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436346
Start	55334408:55334408(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2413delA
AA Mutation	p.Ile805TyrfsTer6(p.I805Yfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436346
Start	55317300:55317300(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3652delA
AA Mutation	p.Met1218CysfsTer4(p.M1218Cfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436346
Start	55334789:55334789(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2032delA
AA Mutation	p.Thr678HisfsTer8(p.T678Hfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436346
Start	55334486:55334486(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2335delA
AA Mutation	p.Ile779SerfsTer4(p.I779Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000436346
Start	55334297:55334297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2524C>T
AA Mutation	p.Arg842Ter(p.R842*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000436346
Start	55334249:55334249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2572A>T
AA Mutation	p.Lys858Ter(p.K858*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436346
Start	55334788:55334789(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs750732366
CDS Mutation	c.2032dupA
AA Mutation	p.Thr678AsnfsTer4(p.T678Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436346
Start	55334485:55334486(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2335dupA
AA Mutation	p.Ile779AsnfsTer7(p.I779Nfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000436346
Start	55343794:55343794(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1189-2delA
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	28
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000436346
Start	55312546:55312547(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3966_3967insATATTTGTT
AA Mutation	p.Glu1322_Glu1323insIlePheVal(p.E1322_E1323insIFV)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript