Colon Cancer: Gene >> WNT11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322563
Start	76187187:76187187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778229304
CDS Mutation	c.943G>A
AA Mutation	p.Gly315Arg(p.G315R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322563
Start	76194721:76194721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.443C>A
AA Mutation	p.Pro148His(p.P148H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322563
Start	76191705:76191705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528803907
CDS Mutation	c.749G>A
AA Mutation	p.Arg250Gln(p.R250Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322563
Start	76191735:76191735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140169859
CDS Mutation	c.719G>A
AA Mutation	p.Arg240Gln(p.R240Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322563
Start	76187078:76187078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1052A>G
AA Mutation	p.Tyr351Cys(p.Y351C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000322563
Start	76196716:76196716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771996935
CDS Mutation	c.86C>T
AA Mutation	p.Ala29Val(p.A29V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322563
Start	76187206:76187206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322563
Start	76191578:76191578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139884639
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322563
Start	76194648:76194648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322563
Start	76194623:76194623(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.541delA
AA Mutation	p.Thr181GlnfsTer8(p.T181Qfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322563
Start	76194622:76194623(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.541dupA
AA Mutation	p.Thr181AsnfsTer7(p.T181Nfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> WNT11

No Mutation Annotation!