Colon Cancer: Gene >> LGI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371418
Start	93797330:93797330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1201C>A
AA Mutation	p.Leu401Met(p.L401M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371418
Start	93797550:93797550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1421G>A
AA Mutation	p.Arg474Gln(p.R474Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371418
Start	93758798:93758798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254G>A
AA Mutation	p.Gly85Glu(p.G85E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371418
Start	93792865:93792865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370151711
CDS Mutation	c.626G>A
AA Mutation	p.Arg209His(p.R209H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371418
Start	93758803:93758803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259T>G
AA Mutation	p.Phe87Val(p.F87V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371418
Start	93790136:93790136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.469G>T
AA Mutation	p.Asp157Tyr(p.D157Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371418
Start	93797603:93797603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1474C>A
AA Mutation	p.Leu492Ile(p.L492I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371418
Start	93792876:93792876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637A>G
AA Mutation	p.Ser213Gly(p.S213G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371418
Start	93758228:93758228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371418
Start	93758279:93758279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371418
Start	93797245:93797245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371418
Start	93797548:93797548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1419G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371418
Start	93758192:93758193(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.52dupA
AA Mutation	p.Arg18LysfsTer16(p.R18Kfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LGI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371418
Start	93797727:93797727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543647504
CDS Mutation	c.1598G>A
AA Mutation	p.Arg533His(p.R533H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371418
Start	93797202:93797202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1073C>T
AA Mutation	p.Thr358Ile(p.T358I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript