Mutation

Primary Site >> Stomach Cancer

Gene >> LAMC2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183235654:183235654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2380C>T
AA Mutation	p.Arg794Cys(p.R794C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183240076:183240076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3106G>T
AA Mutation	p.Ala1036Ser(p.A1036S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183220926:183220926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756385275
CDS Mutation	c.605A>G
AA Mutation	p.Tyr202Cys(p.Y202C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183243234:183243234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144652590
CDS Mutation	c.3416G>A
AA Mutation	p.Arg1139Gln(p.R1139Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183232763:183232763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2126G>T
AA Mutation	p.Gly709Val(p.G709V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183232786:183232786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762028260
CDS Mutation	c.2149C>T
AA Mutation	p.Arg717Trp(p.R717W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183220910:183220910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184817147
CDS Mutation	c.589C>T
AA Mutation	p.Arg197Cys(p.R197C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183237466:183237466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2716G>A
AA Mutation	p.Ala906Thr(p.A906T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183226853:183226853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1222G>T
AA Mutation	p.Gly408Trp(p.G408W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183208021:183208021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771609195
CDS Mutation	c.220C>T
AA Mutation	p.Arg74Trp(p.R74W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264144
Start	183220931:183220931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610G>T
AA Mutation	p.Val204Phe(p.V204F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264144
Start	183228444:183228444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1539T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264144
Start	183232321:183232321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1992G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264144
Start	183236478:183236478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548502176
CDS Mutation	c.2475C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264144
Start	183238375:183238375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2823C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264144
Start	183239557:183239557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3063T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264144
Start	183239449:183239449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2955T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264144
Start	183234392:183234393(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2250dupG
AA Mutation	p.Pro751AlafsTer5(p.P751Afs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript