Colon Cancer: Gene >> TOLLIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317204
Start	1295754:1295754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773801820
CDS Mutation	c.74C>T
AA Mutation	p.Thr25Met(p.T25M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317204
Start	1277150:1277150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714G>T
AA Mutation	p.Gln238His(p.Q238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317204
Start	1290268:1290268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325C>T
AA Mutation	p.Pro109Ser(p.P109S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317204
Start	1290378:1290378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215G>A
AA Mutation	p.Arg72His(p.R72H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317204
Start	1295719:1295719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109G>A
AA Mutation	p.Ala37Thr(p.A37T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317204
Start	1295654:1295654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777213812
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317204
Start	1288651:1288651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TOLLIP

No Mutation Annotation!