Colon Cancer: Gene >> TMEM106B

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396667
Start	12231882:12231882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396667
Start	12224338:12224339(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.395_396delAT
AA Mutation	p.Tyr132CysfsTer4(p.Y132Cfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000396667
Start	12214853:12214853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43G>T
AA Mutation	p.Glu15Ter(p.E15*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000396667
Start	12230388:12230388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM106B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396667
Start	12218503:12218503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263G>T
AA Mutation	p.Arg88Ile(p.R88I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396667
Start	12229776:12229776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746430474
CDS Mutation	c.539G>A
AA Mutation	p.Arg180His(p.R180H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396667
Start	12229816:12229816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.579A>G
Mutation Classification	Silent
Feature Type	Transcript