Colon Cancer: Gene >> LLGL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392550
Start	75570430:75570430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1957T>C
AA Mutation	p.Ser653Pro(p.S653P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392550
Start	75573149:75573149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2596G>A
AA Mutation	p.Val866Ile(p.V866I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392550
Start	75573063:75573063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2510C>T
AA Mutation	p.Ala837Val(p.A837V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392550
Start	75573083:75573083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2530C>T
AA Mutation	p.Arg844Trp(p.R844W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392550
Start	75572015:75572015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2411A>G
AA Mutation	p.Asp804Gly(p.D804G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392550
Start	75563454:75563454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754950482
CDS Mutation	c.817G>A
AA Mutation	p.Val273Met(p.V273M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392550
Start	75570236:75570236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755787767
CDS Mutation	c.1855C>T
AA Mutation	p.Arg619Trp(p.R619W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392550
Start	75568998:75568998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1343G>T
AA Mutation	p.Arg448Leu(p.R448L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392550
Start	75563143:75563143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658G>A
AA Mutation	p.Gly220Ser(p.G220S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392550
Start	75569014:75569014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368604286
CDS Mutation	c.1359G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392550
Start	75573058:75573058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755943993
CDS Mutation	c.2505G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000392550
Start	75563330:75563330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LLGL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392550
Start	75569248:75569248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1504G>A
AA Mutation	p.Asp502Asn(p.D502N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392550
Start	75556093:75556093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.123C>A
AA Mutation	p.Ser41Arg(p.S41R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript