Colon Cancer: Gene >> STYK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000075503
Start	10634050:10634050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127G>A
AA Mutation	p.Val43Ile(p.V43I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000075503
Start	10620322:10620322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375423751
CDS Mutation	c.1091G>A
AA Mutation	p.Arg364His(p.R364H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000075503
Start	10627645:10627645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713C>T
AA Mutation	p.Ala238Val(p.A238V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000075503
Start	10631170:10631170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746426634
CDS Mutation	c.326C>T
AA Mutation	p.Pro109Leu(p.P109L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000075503
Start	10624753:10624753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824A>C
AA Mutation	p.Glu275Ala(p.E275A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000075503
Start	10620162:10620162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1251C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000075503
Start	10621962:10621962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748376514
CDS Mutation	c.978G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> STYK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000075503
Start	10620310:10620310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1103C>T
AA Mutation	p.Ala368Val(p.A368V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000075503
Start	10631107:10631107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747238411
CDS Mutation	c.389G>A
AA Mutation	p.Arg130Gln(p.R130Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000075503
Start	10634026:10634026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761803211
CDS Mutation	c.151G>T
AA Mutation	p.Glu51Ter(p.E51*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript