Colon Cancer: Gene >> RPRD1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373433
Start	38033996:38033996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49A>T
AA Mutation	p.Ser17Cys(p.S17C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373433
Start	38057545:38057545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429G>T
AA Mutation	p.Lys143Asn(p.K143N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373433
Start	38059453:38059453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.588T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373433
Start	38048372:38048372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373433
Start	38089835:38089835(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.946delC
AA Mutation	p.Leu316CysfsTer35(p.L316Cfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373433
Start	38059477:38059478(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.616dupC
AA Mutation	p.Gln206ProfsTer19(p.Q206Pfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000373433
Start	38057531:38057531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RPRD1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373433
Start	38089849:38089849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.955G>T
AA Mutation	p.Ala319Ser(p.A319S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript