Colon Cancer: Gene >> FMNL2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000288670
Start	152617190:152617190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1312C>T
AA Mutation	p.Arg438Trp(p.R438W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152561010:152561010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377550607
CDS Mutation	c.571C>T
AA Mutation	p.Arg191Cys(p.R191C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152647853:152647853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755508231
CDS Mutation	c.3227G>A
AA Mutation	p.Arg1076His(p.R1076H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152628394:152628394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2261G>A
AA Mutation	p.Arg754Gln(p.R754Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152607385:152607385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923G>A
AA Mutation	p.Arg308Lys(p.R308K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288670
Start	152581031:152581031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288670
Start	152628347:152628347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2214G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288670
Start	152521955:152521955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000288670
Start	152614911:152614912(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1128dupT
AA Mutation	p.Asp377Ter(p.D377*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FMNL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152647891:152647891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751231036
CDS Mutation	c.3265G>A
AA Mutation	p.Glu1089Lys(p.E1089K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152628471:152628471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2338C>A
AA Mutation	p.Gln780Lys(p.Q780K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152617134:152617134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256A>C
AA Mutation	p.Lys419Thr(p.K419T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152549082:152549082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344G>T
AA Mutation	p.Arg115Ile(p.R115I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152625552:152625552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1952G>A
AA Mutation	p.Arg651Gln(p.R651Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288670
Start	152628458:152628458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2325C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000288670
Start	152521999:152522000(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.180dupA
AA Mutation	p.Trp61MetfsTer6(p.W61Mfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript