Colon Cancer: Gene >> FMNL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49652014:49652014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1522C>A
AA Mutation	p.Pro508Thr(p.P508T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49658448:49658448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599T>G
AA Mutation	p.Val200Gly(p.V200G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49650748:49650748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1928G>A
AA Mutation	p.Arg643His(p.R643H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49651286:49651286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371568850
CDS Mutation	c.1679G>A
AA Mutation	p.Arg560Gln(p.R560Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49647726:49647726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2755G>T
AA Mutation	p.Val919Phe(p.V919F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49656439:49656439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181518753
CDS Mutation	c.850G>A
AA Mutation	p.Glu284Lys(p.E284K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49662045:49662045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.373G>A
AA Mutation	p.Val125Met(p.V125M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49657147:49657147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649C>A
AA Mutation	p.Leu217Ile(p.L217I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49646951:49646951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369272662
CDS Mutation	c.2930G>A
AA Mutation	p.Arg977His(p.R977H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49649057:49649057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2487G>T
AA Mutation	p.Glu829Asp(p.E829D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49649526:49649526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2248A>G
AA Mutation	p.Ile750Val(p.I750V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49649505:49649505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773190923
CDS Mutation	c.2269G>A
AA Mutation	p.Val757Ile(p.V757I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49646946:49646946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2935G>A
AA Mutation	p.Ala979Thr(p.A979T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000335154
Start	49658443:49658443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757430612
CDS Mutation	c.604C>T
AA Mutation	p.Arg202Trp(p.R202W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49657170:49657170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202178648
CDS Mutation	c.626G>A
AA Mutation	p.Arg209His(p.R209H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49648327:49648327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199600439
CDS Mutation	c.2542G>A
AA Mutation	p.Val848Met(p.V848M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49650710:49650710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770930654
CDS Mutation	c.1966C>T
AA Mutation	p.Arg656Cys(p.R656C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335154
Start	49653798:49653798(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1148delG
AA Mutation	p.Gly383ValfsTer11(p.G383Vfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335154
Start	49707136:49707136(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.45delC
AA Mutation	p.Ser16LeufsTer27(p.S16Lfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FMNL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49658466:49658466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770464448
CDS Mutation	c.581G>A
AA Mutation	p.Arg194His(p.R194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49650721:49650721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759732928
CDS Mutation	c.1955G>A
AA Mutation	p.Arg652His(p.R652H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335154
Start	49668495:49668495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186G>T
AA Mutation	p.Lys62Asn(p.K62N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000335154
Start	49648237:49648237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2632G>T
AA Mutation	p.Glu878Ter(p.E878*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript