Mutation

Primary Site >> Stomach Cancer

Gene >> LAMC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183118072:183118072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1916T>A
AA Mutation	p.Leu639His(p.L639H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183116656:183116656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766744194
CDS Mutation	c.1408G>A
AA Mutation	p.Glu470Lys(p.E470K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183108316:183108316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.764G>A
AA Mutation	p.Arg255His(p.R255H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183114549:183114549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150210600
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347Gln(p.R347Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183128709:183128709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3239G>T
AA Mutation	p.Arg1080Met(p.R1080M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183110625:183110625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.992C>T
AA Mutation	p.Ala331Val(p.A331V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183116808:183116808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1469G>A
AA Mutation	p.Arg490Gln(p.R490Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183121875:183121875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753715089
CDS Mutation	c.2143C>T
AA Mutation	p.Leu715Phe(p.L715F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183142720:183142720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771187282
CDS Mutation	c.4760G>A
AA Mutation	p.Arg1587His(p.R1587H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183142555:183142555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4595T>C
AA Mutation	p.Leu1532Pro(p.L1532P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183117334:183117334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141665938
CDS Mutation	c.1579C>T
AA Mutation	p.Arg527Cys(p.R527C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183024045:183024045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329A>G
AA Mutation	p.Asn110Ser(p.N110S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183136397:183136397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749477657
CDS Mutation	c.4126C>T
AA Mutation	p.Arg1376Cys(p.R1376C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183125403:183125403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2654A>C
AA Mutation	p.Asn885Thr(p.N885T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000258341
Start	183103354:183103354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445C>T
AA Mutation	p.Arg149Cys(p.R149C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000258341
Start	183125397:183125397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2648C>T
AA Mutation	p.Ala883Val(p.A883V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258341
Start	183130375:183130375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3312G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258341
Start	183117411:183117411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1656C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258341
Start	183142697:183142697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139212722
CDS Mutation	c.4737C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258341
Start	183114637:183114637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1128C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258341
Start	183110512:183110512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755836526
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258341
Start	183131337:183131337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3525C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258341
Start	183103353:183103353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.444G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258341
Start	183114599:183114599(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1094delG
AA Mutation	p.Gly365AlafsTer42(p.G365Afs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000258341
Start	183128684:183128684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3214G>T
AA Mutation	p.Glu1072Ter(p.E1072*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258341
Start	183125469:183125470(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2723dupT
AA Mutation	p.Leu908PhefsTer13(p.L908Ffs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000258341
Start	183121721:183121721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1991-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	28
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000258341
Start	183110651:183110652(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1018_1019insACAGAAAAACTA
AA Mutation	p.Leu340delinsHisArgLysThrMet(p.L340delinsHRKTM)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript