Colon Cancer: Gene >> CLU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316403
Start	27608948:27608948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236A>T
AA Mutation	p.Lys79Met(p.K79M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316403
Start	27605096:27605096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.657C>G
AA Mutation	p.Phe219Leu(p.F219L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316403
Start	27605262:27605262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.491A>G
AA Mutation	p.Glu164Gly(p.E164G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316403
Start	27599809:27599809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146625005
CDS Mutation	c.1135G>A
AA Mutation	p.Glu379Lys(p.E379K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316403
Start	27599917:27599917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027G>A
AA Mutation	p.Glu343Lys(p.E343K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316403
Start	27606389:27606389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150438413
CDS Mutation	c.382G>A
AA Mutation	p.Val128Ile(p.V128I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000316403
Start	27609086:27609086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98A>G
AA Mutation	p.Glu33Gly(p.E33G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000316403
Start	27609045:27609045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139C>A
AA Mutation	p.Gln47Lys(p.Q47K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316403
Start	27605051:27605051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374744284
CDS Mutation	c.702G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316403
Start	27606390:27606390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373819420
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316403
Start	27606468:27606468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CLU

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316403
Start	27599963:27599963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762416469
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript