Colon Cancer: Gene >> DVL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184170537:184170537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1933C>T
AA Mutation	p.Arg645Cys(p.R645C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184166462:184166462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920T>C
AA Mutation	p.Phe307Ser(p.F307S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184170616:184170616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2012C>T
AA Mutation	p.Pro671Leu(p.P671L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184170087:184170087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1580C>T
AA Mutation	p.Pro527Leu(p.P527L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184170365:184170365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1761G>T
AA Mutation	p.Lys587Asn(p.K587N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313143
Start	184166496:184166496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.954A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313143
Start	184163672:184163672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.177G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313143
Start	184170593:184170593(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs775463109
CDS Mutation	c.1995delC
AA Mutation	p.Met666CysfsTer2(p.M666Cfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DVL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184167991:184167991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1424G>C
AA Mutation	p.Gly475Ala(p.G475A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184165431:184165431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703T>A
AA Mutation	p.Phe235Ile(p.F235I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313143
Start	184164899:184164899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567C>A
AA Mutation	p.Phe189Leu(p.F189L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313143
Start	184166839:184166839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1062G>T
Mutation Classification	Silent
Feature Type	Transcript