Colon Cancer: Gene >> FMNL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331495
Start	45238580:45238580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911A>G
AA Mutation	p.His304Arg(p.H304R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331495
Start	45244871:45244871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2570A>G
AA Mutation	p.Tyr857Cys(p.Y857C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331495
Start	45234114:45234114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.528G>T
AA Mutation	p.Glu176Asp(p.E176D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331495
Start	45245345:45245345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2821G>C
AA Mutation	p.Val941Leu(p.V941L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331495
Start	45236206:45236206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781402859
CDS Mutation	c.685G>A
AA Mutation	p.Val229Ile(p.V229I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331495
Start	45245283:45245283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755479906
CDS Mutation	c.2759G>A
AA Mutation	p.Arg920His(p.R920H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000331495
Start	45241634:45241634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1585G>T
AA Mutation	p.Asp529Tyr(p.D529Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331495
Start	45245928:45245928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3045G>T
AA Mutation	p.Glu1015Asp(p.E1015D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331495
Start	45237318:45237318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761T>C
AA Mutation	p.Val254Ala(p.V254A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331495
Start	45241564:45241564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1515C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331495
Start	45244996:45244996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766134032
CDS Mutation	c.2616G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331495
Start	45232387:45232388(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.240dupC
AA Mutation	p.Ala81ArgfsTer23(p.A81Rfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000331495
Start	45230603:45230603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FMNL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331495
Start	45230683:45230683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.209A>G
AA Mutation	p.Asp70Gly(p.D70G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331495
Start	45238630:45238630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961G>A
AA Mutation	p.Asp321Asn(p.D321N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331495
Start	45244996:45244996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766134032
CDS Mutation	c.2616G>A
Mutation Classification	Silent
Feature Type	Transcript