Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FLT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28427294:28427294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301C>T
AA Mutation	p.Ala434Val(p.A434V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28467079:28467079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212G>T
AA Mutation	p.Ser71Ile(p.S71I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28427872:28427872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750711298
CDS Mutation	c.1156C>T
AA Mutation	p.Arg386Cys(p.R386C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28430076:28430076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1080G>T
AA Mutation	p.Lys360Asn(p.K360N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28434141:28434141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201044311
CDS Mutation	c.593C>T
AA Mutation	p.Thr198Met(p.T198M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28303286:28303286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750346448
CDS Mutation	c.3898G>A
AA Mutation	p.Val1300Ile(p.V1300I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28433919:28433919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755339233
CDS Mutation	c.713G>A
AA Mutation	p.Arg238His(p.R238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28308908:28308908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3655T>A
AA Mutation	p.Phe1219Ile(p.F1219I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28322865:28322865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554058758
CDS Mutation	c.2878G>A
AA Mutation	p.Val960Ile(p.V960I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28312045:28312045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3440T>G
AA Mutation	p.Phe1147Cys(p.F1147C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28389805:28389805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1960A>G
AA Mutation	p.Thr654Ala(p.T654A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28438304:28438304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55974987
CDS Mutation	c.430G>A
AA Mutation	p.Glu144Lys(p.E144K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28321473:28321473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3164G>A
AA Mutation	p.Arg1055Lys(p.R1055K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28327470:28327470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2788C>A
AA Mutation	p.Leu930Ile(p.L930I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28339242:28339242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2414C>A
AA Mutation	p.Pro805His(p.P805H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28390062:28390062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745653714
CDS Mutation	c.1703C>T
AA Mutation	p.Thr568Met(p.T568M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28384934:28384934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2067G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28430061:28430061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145266667
CDS Mutation	c.1095G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28329718:28329718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2604G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28303197:28303197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369030037
CDS Mutation	c.3987G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282397
Start	28322817:28322818(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2925_2926delAA
AA Mutation	p.Leu977GlufsTer2(p.L977Efs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000282397
Start	28438222:28438222(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.512delA
AA Mutation	p.Lys171SerfsTer7(p.K171Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282397
Start	28431306:28431306(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.818delA
AA Mutation	p.Asn273IlefsTer6(p.N273Ifs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000282397
Start	28434177:28434177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557G>A
AA Mutation	p.Trp186Ter(p.W186*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000282397
Start	28433821:28433821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811G>T
AA Mutation	p.Glu271Ter(p.E271*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FLT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28467077:28467077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758936491
CDS Mutation	c.214G>A
AA Mutation	p.Glu72Lys(p.E72K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28357586:28357586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2216C>A
AA Mutation	p.Ser739Tyr(p.S739Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28319465:28319465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142586121
CDS Mutation	c.3244G>A
AA Mutation	p.Val1082Met(p.V1082M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28327476:28327476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2782T>G
AA Mutation	p.Phe928Val(p.F928V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28384960:28384960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2041G>T
AA Mutation	p.Asp681Tyr(p.D681Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28390065:28390065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374335323
CDS Mutation	c.1700C>T
AA Mutation	p.Pro567Leu(p.P567L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282397
Start	28467107:28467120(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.171_184delAGCCCATAAATGGT
AA Mutation	p.Ala58PhefsTer3(p.A58Ffs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000282397
Start	28319531:28319531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374452662
CDS Mutation	c.3178C>T
AA Mutation	p.Arg1060Ter(p.R1060*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript