Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BPIFA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354297
Start	33239809:33239809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327G>T
AA Mutation	p.Lys109Asn(p.K109N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354297
Start	33239888:33239888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765317724
CDS Mutation	c.406G>A
AA Mutation	p.Gly136Ser(p.G136S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354297
Start	33240242:33240242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764093028
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354297
Start	33240311:33240311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354297
Start	33238167:33238167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354297
Start	33238159:33238159(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.269delG
AA Mutation	p.Gly90AspfsTer6(p.G90Dfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BPIFA1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354297
Start	33239887:33239887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533550245
CDS Mutation	c.405C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354297
Start	33242061:33242061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354297
Start	33241433:33241433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630C>A
Mutation Classification	Silent
Feature Type	Transcript