Colon Cancer: Gene >> WDR66

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121923952:121923952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709C>A
AA Mutation	p.Leu237Met(p.L237M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121931798:121931798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800G>A
AA Mutation	p.Arg267Gln(p.R267Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	122003693:122003693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3379A>G
AA Mutation	p.Thr1127Ala(p.T1127A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121999734:121999734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776727712
CDS Mutation	c.3025G>A
AA Mutation	p.Glu1009Lys(p.E1009K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	122003720:122003720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3406C>A
AA Mutation	p.Leu1136Ile(p.L1136I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121960644:121960644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2193G>T
AA Mutation	p.Trp731Cys(p.W731C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121962090:121962090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2420G>T
AA Mutation	p.Arg807Met(p.R807M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	122001541:122001541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3280C>G
AA Mutation	p.Leu1094Val(p.L1094V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121931825:121931825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.827A>G
AA Mutation	p.Tyr276Cys(p.Y276C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121923822:121923822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579A>T
AA Mutation	p.Glu193Asp(p.E193D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	122003708:122003708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3394G>A
AA Mutation	p.Ala1132Thr(p.A1132T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	122001581:122001581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3320C>T
AA Mutation	p.Ala1107Val(p.A1107V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121958462:121958462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762945575
CDS Mutation	c.1921C>A
AA Mutation	p.Leu641Ile(p.L641I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000288912
Start	121958945:121958945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1984G>A
AA Mutation	p.Ala662Thr(p.A662T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121960690:121960690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2239C>T
AA Mutation	p.Leu747Phe(p.L747F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121921669:121921669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364T>A
AA Mutation	p.Ser122Thr(p.S122T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121999909:121999909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3200G>A
AA Mutation	p.Arg1067Gln(p.R1067Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288912
Start	121961983:121961983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755174578
CDS Mutation	c.2313G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288912
Start	121954281:121954281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1482T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288912
Start	121968110:121968110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2712C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288912
Start	121921599:121921599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747074188
CDS Mutation	c.294A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288912
Start	122003707:122003707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202063312
CDS Mutation	c.3393C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288912
Start	121968044:121968044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2646T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000288912
Start	121923859:121923860(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.620_621delAG
AA Mutation	p.Glu207GlyfsTer35(p.E207Gfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000288912
Start	121949017:121949017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1225G>T
AA Mutation	p.Glu409Ter(p.E409*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000288912
Start	121960684:121960684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2233C>T
AA Mutation	p.Arg745Ter(p.R745*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000288912
Start	121923874:121923874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631G>T
AA Mutation	p.Glu211Ter(p.E211*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000288912
Start	121934358:121934358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.998+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WDR66

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121949010:121949010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1218T>A
AA Mutation	p.Asn406Lys(p.N406K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121923694:121923694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451G>T
AA Mutation	p.Asp151Tyr(p.D151Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121960664:121960664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200928405
CDS Mutation	c.2213G>A
AA Mutation	p.Arg738His(p.R738H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121931777:121931777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779C>A
AA Mutation	p.Ser260Tyr(p.S260Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000288912
Start	121921475:121921475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.170C>T
AA Mutation	p.Thr57Met(p.T57M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288912
Start	121999733:121999733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369167840
CDS Mutation	c.3024C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000288912
Start	121921609:121921609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304G>T
AA Mutation	p.Glu102Ter(p.E102*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript