Colon Cancer: Gene >> BPIFA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253362
Start	33169204:33169204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.59C>A
AA Mutation	p.Ser20Tyr(p.S20Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253362
Start	33178181:33178181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750572385
CDS Mutation	c.598G>A
AA Mutation	p.Val200Met(p.V200M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253362
Start	33175495:33175495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499C>T
AA Mutation	p.Pro167Ser(p.P167S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253362
Start	33169263:33169263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118C>A
AA Mutation	p.Leu40Ile(p.L40I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BPIFA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253362
Start	33178206:33178206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.623T>C
AA Mutation	p.Val208Ala(p.V208A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253362
Start	33169284:33169284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139G>A
AA Mutation	p.Val47Ile(p.V47I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript