Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PDGFRB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150123103:150123103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749226501
CDS Mutation	c.2122C>T
AA Mutation	p.Arg708Cys(p.R708C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150118765:150118765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2886G>C
AA Mutation	p.Leu962Phe(p.L962F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150134980:150134980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401A>G
AA Mutation	p.Glu134Gly(p.E134G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150134908:150134908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.473T>A
AA Mutation	p.Val158Glu(p.V158E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150133741:150133741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753192549
CDS Mutation	c.779C>T
AA Mutation	p.Pro260Leu(p.P260L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150132910:150132910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967G>T
AA Mutation	p.Gly323Cys(p.G323C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150117721:150117721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757545741
CDS Mutation	c.3034G>A
AA Mutation	p.Val1012Met(p.V1012M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150134960:150134960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421G>A
AA Mutation	p.Glu141Lys(p.E141K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150125462:150125462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1790G>T
AA Mutation	p.Arg597Leu(p.R597L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150115921:150115921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3163T>A
AA Mutation	p.Ser1055Thr(p.S1055T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150124742:150124742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780819031
CDS Mutation	c.1897G>A
AA Mutation	p.Val633Ile(p.V633I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150115791:150115791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151236133
CDS Mutation	c.3293G>A
AA Mutation	p.Arg1098Gln(p.R1098Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150135608:150135608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311A>G
AA Mutation	p.Asp104Gly(p.D104G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150115809:150115809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146614144
CDS Mutation	c.3275C>T
AA Mutation	p.Ser1092Leu(p.S1092L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150125565:150125565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1687G>A
AA Mutation	p.Glu563Lys(p.E563K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150129838:150129838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776914915
CDS Mutation	c.1498G>A
AA Mutation	p.Val500Met(p.V500M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150137031:150137031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150173975
CDS Mutation	c.17C>T
AA Mutation	p.Ala6Val(p.A6V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150119482:150119482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2783A>G
AA Mutation	p.His928Arg(p.H928R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150124348:150124348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1925G>A
AA Mutation	p.Ser642Asn(p.S642N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261799
Start	150135778:150135778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754041602
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261799
Start	150129940:150129940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139553770
CDS Mutation	c.1396C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261799
Start	150125476:150125476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367951719
CDS Mutation	c.1776G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261799
Start	150117698:150117698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769027565
CDS Mutation	c.3057C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261799
Start	150122025:150122025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192355633
CDS Mutation	c.2199C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261799
Start	150137036:150137036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138641101
CDS Mutation	c.12G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261799
Start	150134876:150134876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368667212
CDS Mutation	c.505C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261799
Start	150135679:150135679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371465014
CDS Mutation	c.240C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261799
Start	150117629:150117629(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3126delC
AA Mutation	p.Ser1043AlafsTer2(p.S1043Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261799
Start	150135806:150135806(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.113delC
AA Mutation	p.Pro38ArgfsTer15(p.P38Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000261799
Start	150124726:150124726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1912+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PDGFRB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150120917:150120917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778844346
CDS Mutation	c.2557C>T
AA Mutation	p.Arg853Trp(p.R853W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261799
Start	150134938:150134938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.443C>T
AA Mutation	p.Pro148Leu(p.P148L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261799
Start	150120055:150120055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144234864
CDS Mutation	c.2655C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261799
Start	150115814:150115814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183852315
CDS Mutation	c.3270G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261799
Start	150135806:150135806(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.113delC
AA Mutation	p.Pro38ArgfsTer15(p.P38Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000261799
Start	150135630:150135630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289G>T
AA Mutation	p.Glu97Ter(p.E97*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript