Colon Cancer: Gene >> BNIP3L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380629
Start	26391365:26391365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.223C>A
AA Mutation	p.Leu75Ile(p.L75I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000380629
Start	26395232:26395232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287C>A
AA Mutation	p.Pro96His(p.P96H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380629
Start	26408321:26408321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556C>A
AA Mutation	p.Leu186Met(p.L186M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380629
Start	26408080:26408080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380629
Start	26391368:26391368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.226T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380629
Start	26408056:26408056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767130233
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380629
Start	26391305:26391305(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.168delG
AA Mutation	p.Leu57TrpfsTer69(p.L57Wfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BNIP3L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380629
Start	26408087:26408087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445G>A
AA Mutation	p.Glu149Lys(p.E149K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380629
Start	26395236:26395236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373730069
CDS Mutation	c.291G>A
Mutation Classification	Silent
Feature Type	Transcript