Mutation

Primary Site >> Stomach Cancer

Gene >> LMNA

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156138660:156138660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs13768
CDS Mutation	c.1871G>A
AA Mutation	p.Arg624His(p.R624H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156130636:156130636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376G>A
AA Mutation	p.Asp126Asn(p.D126N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156138537:156138537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs59601651
CDS Mutation	c.1748C>T
AA Mutation	p.Ser583Leu(p.S583L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156136952:156136952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267607578
CDS Mutation	c.1412G>A
AA Mutation	p.Arg471His(p.R471H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156138680:156138680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1891G>A
AA Mutation	p.Gly631Ser(p.G631S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156135263:156135263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887G>A
AA Mutation	p.Arg296His(p.R296H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156136252:156136252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267607563
CDS Mutation	c.1196G>A
AA Mutation	p.Arg399His(p.R399H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368300
Start	156135234:156135234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368300
Start	156134936:156134936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368300
Start	156138675:156138676(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs770335541
CDS Mutation	c.1892dupG
AA Mutation	p.Ser632GlnfsTer72(p.S632Qfs*72)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368300
Start	156136224:156136225(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1173dupC
AA Mutation	p.Ser392GlnfsTer34(p.S392Qfs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000368300
Start	156137030:156137030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1488+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000368300
Start	156138659:156138667(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1875_1883delCTACCGCAG
AA Mutation	p.Tyr626_Ser628del(p.Y626_S628del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript