Mutation

Primary Site >> Stomach Cancer

Gene >> CDC20

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310955
Start	43361214:43361214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1172C>T
AA Mutation	p.Ala391Val(p.A391V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310955
Start	43362963:43362963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1334G>A
AA Mutation	p.Arg445Gln(p.R445Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310955
Start	43362978:43362978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1349C>T
AA Mutation	p.Thr450Ile(p.T450I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310955
Start	43363062:43363062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200349485
CDS Mutation	c.1433C>T
AA Mutation	p.Ala478Val(p.A478V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310955
Start	43359314:43359314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310955
Start	43360543:43360543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.798T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310955
Start	43360233:43360233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756975924
CDS Mutation	c.597C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310955
Start	43359275:43359275(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.63delC
AA Mutation	p.Asn22MetfsTer74(p.N22Mfs*74)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000310955
Start	43359258:43359258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43C>T
AA Mutation	p.Gln15Ter(p.Q15*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000310955
Start	43359968:43359968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript