Mutation

Primary Site >> Stomach Cancer

Gene >> TRIM46

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334634
Start	155179662:155179662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755118081
CDS Mutation	c.1316G>A
AA Mutation	p.Arg439His(p.R439H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334634
Start	155175632:155175632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767748060
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Trp(p.R104W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334634
Start	155182091:155182091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1828G>A
AA Mutation	p.Gly610Arg(p.G610R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334634
Start	155181969:155181969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763700927
CDS Mutation	c.1706G>A
AA Mutation	p.Arg569Gln(p.R569Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334634
Start	155175633:155175633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311G>A
AA Mutation	p.Arg104Gln(p.R104Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334634
Start	155182016:155182016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1753G>A
AA Mutation	p.Val585Met(p.V585M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334634
Start	155178233:155178233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1141G>A
AA Mutation	p.Ala381Thr(p.A381T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334634
Start	155176995:155176995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733G>T
AA Mutation	p.Val245Leu(p.V245L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334634
Start	155179736:155179736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1390G>C
AA Mutation	p.Val464Leu(p.V464L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334634
Start	155182012:155182012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1749C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334634
Start	155182087:155182087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1824C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334634
Start	155183854:155183854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1944G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334634
Start	155175487:155175487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334634
Start	155182027:155182027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1764C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334634
Start	155179636:155179636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1290T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334634
Start	155179702:155179702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1356G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334634
Start	155183905:155183905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760539341
CDS Mutation	c.1995G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334634
Start	155178025:155178025(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.934delG
AA Mutation	p.Glu312ArgfsTer107(p.E312Rfs*107)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334634
Start	155179703:155179703(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1363delC
AA Mutation	p.His455IlefsTer32(p.H455Ifs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334634
Start	155176017:155176017(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.457delC
AA Mutation	p.Leu153TrpfsTer12(p.L153Wfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript