Colon Cancer: Gene >> STK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372806
Start	44978464:44978464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138A>C
AA Mutation	p.Lys46Asn(p.K46N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372806
Start	44997283:44997283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.808G>A
AA Mutation	p.Ala270Thr(p.A270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372806
Start	44981894:44981894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311A>G
AA Mutation	p.Tyr104Cys(p.Y104C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372806
Start	45075076:45075076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1364T>C
AA Mutation	p.Met455Thr(p.M455T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372806
Start	45001209:45001209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003G>T
AA Mutation	p.Gly335Cys(p.G335C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372806
Start	45000411:45000411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851C>T
AA Mutation	p.Ala284Val(p.A284V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372806
Start	44987186:44987186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415T>C
AA Mutation	p.Tyr139His(p.Y139H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372806
Start	44997244:44997244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769T>A
AA Mutation	p.Phe257Ile(p.F257I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372806
Start	45000499:45000499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.939C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000372806
Start	45001200:45001200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.994C>T
AA Mutation	p.Arg332Ter(p.R332*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000372806
Start	44981926:44981926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751997042
CDS Mutation	c.343C>T
AA Mutation	p.Arg115Ter(p.R115*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> STK4

No Mutation Annotation!