Colon Cancer: Gene >> WDR13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376729
Start	48602086:48602086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034G>A
AA Mutation	p.Arg345His(p.R345H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376729
Start	48599595:48599595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.401G>A
AA Mutation	p.Gly134Asp(p.G134D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376729
Start	48598904:48598904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229G>T
AA Mutation	p.Ala77Ser(p.A77S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376729
Start	48598922:48598922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.247G>A
AA Mutation	p.Val83Ile(p.V83I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376729
Start	48600330:48600330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782245413
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Cys(p.R179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376729
Start	48600336:48600336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541G>A
AA Mutation	p.Ala181Thr(p.A181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376729
Start	48604918:48604918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1344G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376729
Start	48601894:48601894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376729
Start	48604897:48604897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782614484
CDS Mutation	c.1323G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376729
Start	48598813:48598813(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.143delC
AA Mutation	p.Pro48GlnfsTer8(p.P48Qfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000376729
Start	48598715:48598715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WDR13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376729
Start	48599398:48599398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328C>T
AA Mutation	p.Arg110Cys(p.R110C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376729
Start	48598886:48598886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211G>A
AA Mutation	p.Glu71Lys(p.E71K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376729
Start	48601914:48601914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962C>T
AA Mutation	p.Ala321Val(p.A321V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376729
Start	48598836:48598836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161A>G
AA Mutation	p.Tyr54Cys(p.Y54C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376729
Start	48601849:48601849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376729
Start	48602081:48602081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376729
Start	48601843:48601843(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.896delG
AA Mutation	p.Gly299AlafsTer5(p.G299Afs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript