Colon Cancer: Gene >> TMBIM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258412
Start	218277057:218277057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682A>G
AA Mutation	p.Ile228Val(p.I228V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258412
Start	218275482:218275482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143173370
CDS Mutation	c.929G>A
AA Mutation	p.Arg310His(p.R310H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258412
Start	218277032:218277032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.707T>C
AA Mutation	p.Val236Ala(p.V236A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258412
Start	218276048:218276048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767T>C
AA Mutation	p.Leu256Pro(p.L256P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258412
Start	218280047:218280047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258412
Start	218279336:218279336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258412
Start	218280110:218280110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.219T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TMBIM1

No Mutation Annotation!