Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PHF21B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313237
Start	44913848:44913848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755504448
CDS Mutation	c.805C>T
AA Mutation	p.Arg269Trp(p.R269W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313237
Start	44887980:44887980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1180C>T
AA Mutation	p.Pro394Ser(p.P394S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313237
Start	44920414:44920414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.197C>T
AA Mutation	p.Ala66Val(p.A66V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313237
Start	44888045:44888045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1115G>A
AA Mutation	p.Gly372Glu(p.G372E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313237
Start	44916541:44916541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000313237
Start	44883205:44883205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1477C>T
AA Mutation	p.Gln493Ter(p.Q493*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PHF21B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313237
Start	44913910:44913910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776556694
CDS Mutation	c.743C>T
AA Mutation	p.Ser248Leu(p.S248L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313237
Start	44916528:44916528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767031532
CDS Mutation	c.316G>A
AA Mutation	p.Val106Ile(p.V106I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313237
Start	44916590:44916590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.254C>A
AA Mutation	p.Ala85Asp(p.A85D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript