Mutation

Primary Site >> Stomach Cancer

Gene >> DLGAP3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34868683:34868683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776746778
CDS Mutation	c.2407C>T
AA Mutation	p.Arg803Trp(p.R803W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34904452:34904452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141061512
CDS Mutation	c.932G>A
AA Mutation	p.Arg311His(p.R311H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34869073:34869073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764135834
CDS Mutation	c.2017C>T
AA Mutation	p.Arg673Cys(p.R673C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34866130:34866130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2893G>A
AA Mutation	p.Ala965Thr(p.A965T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34904465:34904465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778851121
CDS Mutation	c.919G>A
AA Mutation	p.Gly307Arg(p.G307R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34904485:34904485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899G>A
AA Mutation	p.Ser300Asn(p.S300N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34904717:34904717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.667C>A
AA Mutation	p.His223Asn(p.H223N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34904617:34904617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767A>G
AA Mutation	p.Lys256Arg(p.K256R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34866211:34866211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2812C>T
AA Mutation	p.Arg938Trp(p.R938W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34900150:34900150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146586197
CDS Mutation	c.1231G>A
AA Mutation	p.Gly411Ser(p.G411S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235180
Start	34904817:34904817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235180
Start	34867120:34867120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771631823
CDS Mutation	c.2649C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235180
Start	34904793:34904793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759351971
CDS Mutation	c.591G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235180
Start	34904343:34904343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754381123
CDS Mutation	c.1041C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235180
Start	34904292:34904292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1092T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235180
Start	34868720:34868720(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2370delC
AA Mutation	p.Cys791AlafsTer96(p.C791Afs*96)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235180
Start	34900251:34900251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1130delG
AA Mutation	p.Gly377ValfsTer91(p.G377Vfs*91)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235180
Start	34899713:34899713(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1342delC
AA Mutation	p.Arg448GlyfsTer20(p.R448Gfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000235180
Start	34904957:34904957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427C>T
AA Mutation	p.Arg143Ter(p.R143*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000235180
Start	34904399:34904399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985C>T
AA Mutation	p.Arg329Ter(p.R329*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000235180
Start	34869090:34869090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2001-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript