Mutation

Primary Site >> Stomach Cancer

Gene >> LTBP3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65557649:65557649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311C>T
AA Mutation	p.Thr104Met(p.T104M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65543168:65543168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2533A>T
AA Mutation	p.Asn845Tyr(p.N845Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65554314:65554314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398C>T
AA Mutation	p.Pro133Leu(p.P133L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65554281:65554281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746544643
CDS Mutation	c.431C>T
AA Mutation	p.Ala144Val(p.A144V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65540918:65540918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2930A>G
AA Mutation	p.Tyr977Cys(p.Y977C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65552281:65552281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368676768
CDS Mutation	c.1312G>A
AA Mutation	p.Ala438Thr(p.A438T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65554057:65554057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655G>A
AA Mutation	p.Ala219Thr(p.A219T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65552373:65552373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147206443
CDS Mutation	c.1220G>A
AA Mutation	p.Arg407His(p.R407H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65548018:65548018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1748A>G
AA Mutation	p.Asn583Ser(p.N583S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65552979:65552979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1067T>C
AA Mutation	p.Ile356Thr(p.I356T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301873
Start	65547703:65547703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747104260
CDS Mutation	c.1965G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301873
Start	65547536:65547536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2010C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301873
Start	65548008:65548008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1758C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301873
Start	65547470:65547470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2076G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301873
Start	65554364:65554364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301873
Start	65552081:65552081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111330939
CDS Mutation	c.1422C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301873
Start	65557717:65557717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301873
Start	65546812:65546812(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs752375653
CDS Mutation	c.2216delG
AA Mutation	p.Gly739AlafsTer7(p.G739Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301873
Start	65547703:65547703(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1965delG
AA Mutation	p.Arg656AlafsTer6(p.R656Afs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301873
Start	65541144:65541145(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2874_2875insA
AA Mutation	p.Cys959MetfsTer35(p.C959Mfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301873
Start	65546811:65546812(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2216dupG
AA Mutation	p.Gly740ArgfsTer51(p.G740Rfs*51)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	22
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000301873
Start	65539629:65539629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3548-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript