Colon Cancer: Gene >> FTO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000471389
Start	53826299:53826299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577569584
CDS Mutation	c.559G>A
AA Mutation	p.Gly187Arg(p.G187R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000471389
Start	53826263:53826263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523G>T
AA Mutation	p.Asp175Tyr(p.D175Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000471389
Start	53826018:53826018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151263395
CDS Mutation	c.278C>T
AA Mutation	p.Pro93Leu(p.P93L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000471389
Start	53873813:53873813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923G>T
AA Mutation	p.Cys308Phe(p.C308F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000471389
Start	53879878:53879878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761330347
CDS Mutation	c.1010G>A
AA Mutation	p.Arg337His(p.R337H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000471389
Start	53826030:53826030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290T>G
AA Mutation	p.Ile97Ser(p.I97S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000471389
Start	54111788:54111788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1391T>C
AA Mutation	p.Leu464Ser(p.L464S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000471389
Start	53810204:53810204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.110A>C
AA Mutation	p.Glu37Ala(p.E37A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000471389
Start	53888932:53888932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220G>T
AA Mutation	p.Trp407Leu(p.W407L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000471389
Start	53844192:53844192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.789A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000471389
Start	53826298:53826298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45492996
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000471389
Start	53873854:53873854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200201735
CDS Mutation	c.964C>T
AA Mutation	p.Arg322Ter(p.R322*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FTO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000471389
Start	53825941:53825941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201A>T
AA Mutation	p.Glu67Asp(p.E67D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000471389
Start	53826125:53826125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751544648
CDS Mutation	c.385G>A
AA Mutation	p.Glu129Lys(p.E129K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000471389
Start	54111777:54111777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1380T>A
Mutation Classification	Silent
Feature Type	Transcript