Colon Cancer: Gene >> DBN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309007
Start	177466957:177466957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661C>T
AA Mutation	p.Arg221Cys(p.R221C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309007
Start	177466989:177466989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629G>A
AA Mutation	p.Arg210Gln(p.R210Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309007
Start	177459164:177459164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753006714
CDS Mutation	c.1060C>T
AA Mutation	p.Arg354Trp(p.R354W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309007
Start	177459158:177459158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066C>A
AA Mutation	p.Leu356Met(p.L356M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309007
Start	177457474:177457474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1909C>G
AA Mutation	p.Pro637Ala(p.P637A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309007
Start	177458554:177458554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1280C>T
AA Mutation	p.Ala427Val(p.A427V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309007
Start	177458499:177458499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1335G>T
AA Mutation	p.Glu445Asp(p.E445D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309007
Start	177466955:177466955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372439938
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309007
Start	177458433:177458433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748601855
CDS Mutation	c.1401C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309007
Start	177458118:177458118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1716G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DBN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309007
Start	177459217:177459217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144418852
CDS Mutation	c.1007G>A
AA Mutation	p.Arg336Gln(p.R336Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309007
Start	177460508:177460508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.879C>A
AA Mutation	p.Phe293Leu(p.F293L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript