Colon Cancer: Gene >> WDR19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39268079:39268079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3346G>A
AA Mutation	p.Glu1116Lys(p.E1116K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39268013:39268013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757564170
CDS Mutation	c.3280C>T
AA Mutation	p.Arg1094Cys(p.R1094C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39244547:39244547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2640G>T
AA Mutation	p.Lys880Asn(p.K880N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39216100:39216100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1139T>A
AA Mutation	p.Leu380Gln(p.L380Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39253264:39253264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2848T>A
AA Mutation	p.Ser950Thr(p.S950T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39270065:39270065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3448A>G
AA Mutation	p.Asn1150Asp(p.N1150D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39234826:39234826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2314G>T
AA Mutation	p.Asp772Tyr(p.D772Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39255933:39255933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3087C>A
AA Mutation	p.Phe1029Leu(p.F1029L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39218005:39218005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1379C>T
AA Mutation	p.Ala460Val(p.A460V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39228287:39228287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1707T>G
AA Mutation	p.Asp569Glu(p.D569E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399820
Start	39274857:39274857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202102903
CDS Mutation	c.3615C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399820
Start	39272989:39272989(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3497delA
AA Mutation	p.Asn1166MetfsTer5(p.N1166Mfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000399820
Start	39278563:39278563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3942T>A
AA Mutation	p.Cys1314Ter(p.C1314*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000399820
Start	39185781:39185781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62G>A
AA Mutation	p.Trp21Ter(p.W21*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399820
Start	39205183:39205184(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.641dupT
AA Mutation	p.Leu214PhefsTer5(p.L214Ffs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399820
Start	39205183:39205184(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.640_641dupTT
AA Mutation	p.Leu214PhefsTer2(p.L214Ffs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399820
Start	39185783:39185784(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs769095843
CDS Mutation	c.70dupA
AA Mutation	p.Thr24AsnfsTer12(p.T24Nfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> WDR19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39228336:39228336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1756T>A
AA Mutation	p.Phe586Ile(p.F586I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399820
Start	39215888:39215888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1009T>C
AA Mutation	p.Ser337Pro(p.S337P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399820
Start	39254014:39254014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2985C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399820
Start	39186569:39186569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399820
Start	39205180:39205180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000399820
Start	39186588:39186588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148G>T
AA Mutation	p.Glu50Ter(p.E50*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000399820
Start	39228306:39228307(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1727_1728insCGA
AA Mutation	p.Asp579dup(p.D579dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript