Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LMNA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156135950:156135950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397517913
CDS Mutation	c.986G>A
AA Mutation	p.Arg329His(p.R329H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156115072:156115072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397517895
CDS Mutation	c.154C>G
AA Mutation	p.Leu52Val(p.L52V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156130726:156130726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760743233
CDS Mutation	c.466C>T
AA Mutation	p.Arg156Cys(p.R156C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368300
Start	156136379:156136379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1323C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368300
Start	156136352:156136352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1296G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LMNA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156134857:156134857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760388350
CDS Mutation	c.692A>G
AA Mutation	p.Asn231Ser(p.N231S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000368300
Start	156137027:156137027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200466188
CDS Mutation	c.1487C>T
AA Mutation	p.Thr496Met(p.T496M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368300
Start	156138593:156138593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs60662302
CDS Mutation	c.1804G>A
AA Mutation	p.Gly602Ser(p.G602S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript