Colon Cancer: Gene >> FILIP1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99850363:99850363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1313A>C
AA Mutation	p.Lys438Thr(p.K438T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99849433:99849433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2243A>C
AA Mutation	p.Lys748Thr(p.K748T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99850642:99850642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374961168
CDS Mutation	c.1034G>A
AA Mutation	p.Arg345Gln(p.R345Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99930935:99930935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.86A>T
AA Mutation	p.Lys29Ile(p.K29I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99849594:99849594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2082G>T
AA Mutation	p.Glu694Asp(p.E694D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99850039:99850039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373504477
CDS Mutation	c.1637C>T
AA Mutation	p.Ala546Val(p.A546V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99931017:99931017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766701827
CDS Mutation	c.4C>T
AA Mutation	p.Arg2Cys(p.R2C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99850786:99850786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.890C>T
AA Mutation	p.Thr297Met(p.T297M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99850243:99850243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776850792
CDS Mutation	c.1433G>A
AA Mutation	p.Arg478Gln(p.R478Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99850426:99850426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250T>C
AA Mutation	p.Val417Ala(p.V417A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99924401:99924401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434A>C
AA Mutation	p.Lys145Thr(p.K145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99850691:99850691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371794170
CDS Mutation	c.985G>A
AA Mutation	p.Ala329Thr(p.A329T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99848447:99848447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3229C>A
AA Mutation	p.Pro1077Thr(p.P1077T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99850329:99850329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1347A>C
AA Mutation	p.Glu449Asp(p.E449D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99849335:99849335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2341C>A
AA Mutation	p.Leu781Ile(p.L781I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354552
Start	99848871:99848871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2805G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354552
Start	99929904:99929904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200563011
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354552
Start	99848907:99848907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373124183
CDS Mutation	c.2769C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354552
Start	99849095:99849095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2581C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354552
Start	99849096:99849096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2580G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354552
Start	99849658:99849658(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2018delT
AA Mutation	p.Leu673TyrfsTer5(p.L673Yfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000354552
Start	99924381:99924381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454G>T
AA Mutation	p.Glu152Ter(p.E152*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000354552
Start	99851025:99851027(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.649_651delAAG
AA Mutation	p.Lys217del(p.K217del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FILIP1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99848648:99848648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3028T>G
AA Mutation	p.Ser1010Ala(p.S1010A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99849149:99849149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2527T>G
AA Mutation	p.Ser843Ala(p.S843A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354552
Start	99930979:99930979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42G>T
AA Mutation	p.Lys14Asn(p.K14N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000354552
Start	99924285:99924285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550G>T
AA Mutation	p.Glu184Ter(p.E184*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354552
Start	99850603:99850604(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1072dupA
AA Mutation	p.Ile358AsnfsTer3(p.I358Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript