Colon Cancer: Gene >> WRAP73

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270708
Start	3635019:3635019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.794C>T
AA Mutation	p.Ala265Val(p.A265V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270708
Start	3635071:3635071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774325847
CDS Mutation	c.742C>T
AA Mutation	p.Arg248Cys(p.R248C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270708
Start	3638818:3638818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548238349
CDS Mutation	c.344G>A
AA Mutation	p.Arg115Gln(p.R115Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270708
Start	3633442:3633442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199984886
CDS Mutation	c.878C>T
AA Mutation	p.Pro293Leu(p.P293L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270708
Start	3630979:3630979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1379C>T
AA Mutation	p.Thr460Met(p.T460M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270708
Start	3637065:3637065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780375041
CDS Mutation	c.446C>T
AA Mutation	p.Ala149Val(p.A149V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000270708
Start	3646695:3646695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774325760
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Cys(p.R104C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000270708
Start	3637053:3637053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142980544
CDS Mutation	c.458G>A
AA Mutation	p.Arg153Gln(p.R153Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270708
Start	3635995:3635995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270708
Start	3631092:3631092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1266C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270708
Start	3631071:3631071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114827156
CDS Mutation	c.1287G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270708
Start	3632331:3632331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543992674
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270708
Start	3647435:3647435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768787313
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WRAP73

No Mutation Annotation!