Mutation

Primary Site >> Stomach Cancer

Gene >> LAMB3

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356082
Start	209634447:209634447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564G>C
AA Mutation	p.Lys188Asn(p.K188N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209630720:209630720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838G>A
AA Mutation	p.Val280Ile(p.V280I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209634520:209634520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754855375
CDS Mutation	c.491G>A
AA Mutation	p.Arg164Gln(p.R164Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209632696:209632696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761752478
CDS Mutation	c.709G>A
AA Mutation	p.Ala237Thr(p.A237T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209625766:209625766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1858C>A
AA Mutation	p.Leu620Met(p.L620M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209627522:209627522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346G>A
AA Mutation	p.Gly449Glu(p.G449E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209630642:209630642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916G>A
AA Mutation	p.Glu306Lys(p.E306K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209625700:209625700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767931599
CDS Mutation	c.1924G>A
AA Mutation	p.Ala642Thr(p.A642T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209633093:209633093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605C>T
AA Mutation	p.Ala202Val(p.A202V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209638611:209638611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221C>A
AA Mutation	p.Pro74His(p.P74H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209623658:209623658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2205C>A
AA Mutation	p.Ser735Arg(p.S735R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209625663:209625663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1961C>T
AA Mutation	p.Ala654Val(p.A654V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209625936:209625936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753850608
CDS Mutation	c.1688G>A
AA Mutation	p.Arg563His(p.R563H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209625987:209625987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1637G>A
AA Mutation	p.Cys546Tyr(p.C546Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209634517:209634517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.494C>A
AA Mutation	p.Pro165His(p.P165H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209637959:209637959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.321G>C
AA Mutation	p.Gln107His(p.Q107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209634529:209634529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752418863
CDS Mutation	c.482G>A
AA Mutation	p.Arg161His(p.R161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356082
Start	209625648:209625648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1976G>T
AA Mutation	p.Arg659Met(p.R659M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356082
Start	209623998:209623998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375951428
CDS Mutation	c.1979G>A
AA Mutation	p.Arg660Gln(p.R660Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209623905:209623905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777788000
CDS Mutation	c.2072G>A
AA Mutation	p.Gly691Asp(p.G691D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209629787:209629787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082A>T
AA Mutation	p.His361Leu(p.H361L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356082
Start	209615364:209615364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753454602
CDS Mutation	c.3426G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356082
Start	209638580:209638580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.252T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356082
Start	209625782:209625782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1842G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356082
Start	209625890:209625890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138710333
CDS Mutation	c.1734C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356082
Start	209626957:209626957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1507C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356082
Start	209627428:209627428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779846779
CDS Mutation	c.1440G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356082
Start	209617475:209617475(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3163delG
AA Mutation	p.Ala1055GlnfsTer18(p.A1055Qfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356082
Start	209629857:209629857(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1012delG
AA Mutation	p.Ala338HisfsTer58(p.A338Hfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356082
Start	209649975:209649975(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.172delC
AA Mutation	p.Gln58SerfsTer7(p.Q58Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000356082
Start	209625982:209625982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1642A>T
AA Mutation	p.Lys548Ter(p.K548*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000356082
Start	209623948:209623950(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2027_2029delTGT
AA Mutation	p.Leu676del(p.L676del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript