Colon Cancer: Gene >> FMO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171103946:171103946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294G>T
AA Mutation	p.Lys98Asn(p.K98N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171114162:171114162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983C>T
AA Mutation	p.Ala328Val(p.A328V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171116217:171116217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1193C>A
AA Mutation	p.Thr398Asn(p.T398N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171108216:171108216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622G>A
AA Mutation	p.Glu208Lys(p.E208K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171110876:171110876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201271626
CDS Mutation	c.706G>A
AA Mutation	p.Val236Ile(p.V236I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171103850:171103850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72549323
CDS Mutation	c.198G>T
AA Mutation	p.Met66Ile(p.M66I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171117390:171117390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547A>G
AA Mutation	p.Lys516Arg(p.K516R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171114218:171114218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039A>G
AA Mutation	p.Asn347Asp(p.N347D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171092754:171092754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.96G>T
AA Mutation	p.Glu32Asp(p.E32D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171114050:171114050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871A>C
AA Mutation	p.Ser291Arg(p.S291R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171117373:171117373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1530C>A
AA Mutation	p.Phe510Leu(p.F510L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171117354:171117354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754517205
CDS Mutation	c.1511G>T
AA Mutation	p.Arg504Ile(p.R504I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367755
Start	171092670:171092670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367755
Start	171117418:171117418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1575C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367755
Start	171114235:171114235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1056A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367755
Start	171116267:171116267(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1247delA
AA Mutation	p.Lys416SerfsTer72(p.K416Sfs*72)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000367755
Start	171107759:171107759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780703747
CDS Mutation	c.406G>T
AA Mutation	p.Glu136Ter(p.E136*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367755
Start	171114076:171114077(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.897_898insTATAAATTGAT
AA Mutation	p.Lys300TyrfsTer8(p.K300Yfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FMO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171117316:171117316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1473C>A
AA Mutation	p.Asp491Glu(p.D491E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367755
Start	171117373:171117373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1530C>A
AA Mutation	p.Phe510Leu(p.F510L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367755
Start	171114202:171114202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1023T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367755
Start	171107770:171107770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.417C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367755
Start	171114157:171114157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.978C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000367755
Start	171110882:171110882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712C>T
AA Mutation	p.Arg238Ter(p.R238*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript