Colon Cancer: Gene >> FMO5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147201352:147201352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.983T>G
AA Mutation	p.Phe328Cys(p.F328C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147225021:147225021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9G>T
AA Mutation	p.Lys3Asn(p.K3N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147187102:147187102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1400C>A
AA Mutation	p.Pro467His(p.P467H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147201169:147201169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166C>T
AA Mutation	p.Ala389Val(p.A389V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147213433:147213433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362C>T
AA Mutation	p.Ala121Val(p.A121V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147208870:147208870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812G>C
AA Mutation	p.Gly271Ala(p.G271A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147201205:147201205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130C>A
AA Mutation	p.Ala377Asp(p.A377D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147208936:147208936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746G>A
AA Mutation	p.Gly249Asp(p.G249D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254090
Start	147213444:147213444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.351G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254090
Start	147213388:147213388(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.407delA
AA Mutation	p.Lys136ArgfsTer3(p.K136Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254090
Start	147187211:147187211(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1291delG
AA Mutation	p.Asp431ThrfsTer3(p.D431Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FMO5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147215815:147215815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263T>G
AA Mutation	p.Val88Gly(p.V88G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147201461:147201461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874C>A
AA Mutation	p.Arg292Ser(p.R292S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147187048:147187048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376858269
CDS Mutation	c.1454G>A
AA Mutation	p.Arg485Gln(p.R485Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254090
Start	147224929:147224929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.101G>T
AA Mutation	p.Arg34Met(p.R34M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript