Colon Cancer: Gene >> LY6K

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292430
Start	142703178:142703178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.305T>G
AA Mutation	p.Phe102Cys(p.F102C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292430
Start	142700556:142700556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.29T>C
AA Mutation	p.Val10Ala(p.V10A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292430
Start	142700601:142700601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.74A>C
AA Mutation	p.Gln25Pro(p.Q25P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292430
Start	142700595:142700595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68C>T
AA Mutation	p.Ala23Val(p.A23V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292430
Start	142703118:142703118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245C>T
AA Mutation	p.Ala82Val(p.A82V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292430
Start	142703119:142703119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782387825
CDS Mutation	c.246G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LY6K

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292430
Start	142703118:142703118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245C>T
AA Mutation	p.Ala82Val(p.A82V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292430
Start	142703119:142703119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782387825
CDS Mutation	c.246G>A
Mutation Classification	Silent
Feature Type	Transcript