Colon Cancer: Gene >> LLGL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316843
Start	18241661:18241661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2713C>T
AA Mutation	p.Arg905Trp(p.R905W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316843
Start	18241497:18241497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753689203
CDS Mutation	c.2549C>T
AA Mutation	p.Thr850Met(p.T850M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316843
Start	18232675:18232675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775418941
CDS Mutation	c.265C>T
AA Mutation	p.Arg89Cys(p.R89C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316843
Start	18240700:18240700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200044915
CDS Mutation	c.2329G>A
AA Mutation	p.Val777Met(p.V777M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316843
Start	18234913:18234913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150688696
CDS Mutation	c.980G>A
AA Mutation	p.Arg327Gln(p.R327Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316843
Start	18238109:18238109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369186591
CDS Mutation	c.1947G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316843
Start	18236936:18236936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1608C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316843
Start	18242806:18242806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3180C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316843
Start	18230009:18230009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316843
Start	18241982:18241982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753952691
CDS Mutation	c.2865C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316843
Start	18235484:18235485(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1304dupG
AA Mutation	p.Arg436ProfsTer18(p.R436Pfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LLGL1

No Mutation Annotation!