Colon Cancer: Gene >> PFKFB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000232375
Start	48550161:48550161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.171G>T
AA Mutation	p.Lys57Asn(p.K57N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000232375
Start	48523542:48523542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1280C>T
AA Mutation	p.Ala427Val(p.A427V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000232375
Start	48536362:48536362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.734T>C
AA Mutation	p.Ile245Thr(p.I245T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000232375
Start	48539707:48539707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443A>C
AA Mutation	p.Asn148Thr(p.N148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000232375
Start	48539734:48539734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.416C>G
AA Mutation	p.Ala139Gly(p.A139G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000232375
Start	48523771:48523771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1152G>T
AA Mutation	p.Glu384Asp(p.E384D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232375
Start	48523720:48523720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1203C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PFKFB4

No Mutation Annotation!