Colon Cancer: Gene >> FLAD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292180
Start	154983741:154983741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>T
AA Mutation	p.Arg16Met(p.R16M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292180
Start	154993024:154993024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1751A>G
AA Mutation	p.Asn584Ser(p.N584S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292180
Start	154988519:154988519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146501091
CDS Mutation	c.787C>T
AA Mutation	p.Arg263Trp(p.R263W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292180
Start	154992746:154992746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771466122
CDS Mutation	c.1588C>T
AA Mutation	p.Arg530Cys(p.R530C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292180
Start	154988110:154988110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378C>G
AA Mutation	p.His126Gln(p.H126Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292180
Start	154989590:154989590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148C>T
AA Mutation	p.Ala383Val(p.A383V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292180
Start	154988350:154988350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FLAD1

No Mutation Annotation!