Colon Cancer: Gene >> WRAP53

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316024
Start	7688937:7688937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289G>A
AA Mutation	p.Glu97Lys(p.E97K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316024
Start	7688907:7688907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259A>G
AA Mutation	p.Ser87Gly(p.S87G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316024
Start	7702824:7702824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759563684
CDS Mutation	c.1246C>T
AA Mutation	p.Arg416Cys(p.R416C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316024
Start	7703354:7703354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1515G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316024
Start	7703397:7703397(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs755116516
CDS Mutation	c.1564delG
AA Mutation	p.Ala522ArgfsTer26(p.A522Rfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant;stop_lost
Transcription ID	ENST00000316024
Start	7703485:7703485(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.*3delA
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316024
Start	7688855:7688855(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.211delG
AA Mutation	p.Asp71ThrfsTer19(p.D71Tfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> WRAP53

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316024
Start	7688997:7688997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773992093
CDS Mutation	c.349G>A
AA Mutation	p.Glu117Lys(p.E117K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316024
Start	7702835:7702835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140635900
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316024
Start	7688874:7688874(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.226delT
AA Mutation	p.Ser76ProfsTer14(p.S76Pfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript