Colon Cancer: Gene >> TMEM147

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222284
Start	35547135:35547135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446C>T
AA Mutation	p.Ala149Val(p.A149V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222284
Start	35547371:35547371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599C>T
AA Mutation	p.Ala200Val(p.A200V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222284
Start	35547344:35547344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760506450
CDS Mutation	c.572C>T
AA Mutation	p.Ser191Leu(p.S191L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222284
Start	35547434:35547434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662A>G
AA Mutation	p.Asn221Ser(p.N221S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222284
Start	35547435:35547435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.663T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222284
Start	35547387:35547387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546677760
CDS Mutation	c.615G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM147

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222284
Start	35546712:35546712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248G>A
AA Mutation	p.Gly83Asp(p.G83D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript