Colon Cancer: Gene >> WDR81

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1732398:1732398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4231C>T
AA Mutation	p.Arg1411Cys(p.R1411C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1727135:1727135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2176A>G
AA Mutation	p.Asn726Asp(p.N726D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1727631:1727631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531333165
CDS Mutation	c.2672G>A
AA Mutation	p.Arg891His(p.R891H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1732438:1732438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768873196
CDS Mutation	c.4271C>T
AA Mutation	p.Pro1424Leu(p.P1424L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1732709:1732709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749340184
CDS Mutation	c.4367C>A
AA Mutation	p.Pro1456Gln(p.P1456Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1725785:1725785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.826C>T
AA Mutation	p.Arg276Cys(p.R276C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1727508:1727508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2549C>A
AA Mutation	p.Pro850His(p.P850H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1726819:1726819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1860G>T
AA Mutation	p.Glu620Asp(p.E620D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1735607:1735607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770164850
CDS Mutation	c.5215C>T
AA Mutation	p.Arg1739Trp(p.R1739W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1736057:1736057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759169049
CDS Mutation	c.5344G>A
AA Mutation	p.Gly1782Ser(p.G1782S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1726451:1726451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777266380
CDS Mutation	c.1492G>A
AA Mutation	p.Asp498Asn(p.D498N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1727299:1727299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2340G>T
AA Mutation	p.Glu780Asp(p.E780D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1732329:1732329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777833436
CDS Mutation	c.4162C>T
AA Mutation	p.Pro1388Ser(p.P1388S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1725956:1725956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997G>A
AA Mutation	p.Gly333Arg(p.G333R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1734135:1734135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140534402
CDS Mutation	c.5098G>A
AA Mutation	p.Val1700Ile(p.V1700I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409644
Start	1725559:1725559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409644
Start	1727170:1727170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2211G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409644
Start	1733579:1733579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4542G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409644
Start	1734122:1734122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5085G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409644
Start	1726288:1726288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1329C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409644
Start	1726501:1726501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1542G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409644
Start	1733822:1733822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143696120
CDS Mutation	c.4785C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409644
Start	1733996:1733996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374175675
CDS Mutation	c.4959C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409644
Start	1726360:1726360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1401C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409644
Start	1732406:1732406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4239A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409644
Start	1735641:1735641(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5254delC
AA Mutation	p.His1752ThrfsTer33(p.H1752Tfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409644
Start	1732449:1732449(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4286delT
AA Mutation	p.Phe1429SerfsTer15(p.F1429Sfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000409644
Start	1736048:1736048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762607878
CDS Mutation	c.5335C>T
AA Mutation	p.Arg1779Ter(p.R1779*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> WDR81

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1726595:1726595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1636G>A
AA Mutation	p.Asp546Asn(p.D546N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1726565:1726565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1606G>A
AA Mutation	p.Glu536Lys(p.E536K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409644
Start	1734127:1734127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5090G>A
AA Mutation	p.Arg1697His(p.R1697H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript