Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MLKL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308807
Start	74691436:74691436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563T>C
AA Mutation	p.Ile188Thr(p.I188T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308807
Start	74682780:74682780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377446580
CDS Mutation	c.827C>T
AA Mutation	p.Pro276Leu(p.P276L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308807
Start	74695483:74695483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201376894
CDS Mutation	c.275G>A
AA Mutation	p.Ser92Asn(p.S92N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308807
Start	74691282:74691282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308807
Start	74674997:74674997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1344C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308807
Start	74678932:74678932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MLKL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308807
Start	74695600:74695600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.158T>C
AA Mutation	p.Val53Ala(p.V53A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308807
Start	74695493:74695493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265C>A
AA Mutation	p.Leu89Ile(p.L89I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308807
Start	74675009:74675009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1332C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000308807
Start	74692381:74692381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496G>T
AA Mutation	p.Glu166Ter(p.E166*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript