Colon Cancer: Gene >> FMO4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171331711:171331711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767244751
CDS Mutation	c.556C>T
AA Mutation	p.Arg186Cys(p.R186C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171332898:171332898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817A>G
AA Mutation	p.Ile273Val(p.I273V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171341736:171341736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1574C>T
AA Mutation	p.Ala525Val(p.A525V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171332794:171332794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713G>A
AA Mutation	p.Arg238Lys(p.R238K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171332794:171332794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713G>C
AA Mutation	p.Arg238Thr(p.R238T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171334487:171334487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573059844
CDS Mutation	c.904G>A
AA Mutation	p.Val302Met(p.V302M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367749
Start	171334615:171334615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1032C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367749
Start	171331728:171331728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.573T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367749
Start	171334615:171334615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1032C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367749
Start	171341677:171341677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1515C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367749
Start	171334589:171334589(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1011delT
AA Mutation	p.Phe337LeufsTer22(p.F337Lfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367749
Start	171341715:171341715(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1558delG
AA Mutation	p.Ala520HisfsTer18(p.A520Hfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000367749
Start	171331768:171331768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373804650
CDS Mutation	c.613C>T
AA Mutation	p.Arg205Ter(p.R205*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FMO4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171323097:171323097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764211255
CDS Mutation	c.226G>A
AA Mutation	p.Glu76Lys(p.E76K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171334512:171334512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929C>T
AA Mutation	p.Ala310Val(p.A310V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171319837:171319837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12A>C
AA Mutation	p.Lys4Asn(p.K4N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171324271:171324271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.455A>G
AA Mutation	p.Asn152Ser(p.N152S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171341562:171341562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1400C>A
AA Mutation	p.Thr467Asn(p.T467N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367749
Start	171341825:171341825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1663C>A
AA Mutation	p.Leu555Ile(p.L555I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript