Colon Cancer: Gene >> APOBEC3C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361441
Start	39015666:39015666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.89G>A
AA Mutation	p.Arg30Gln(p.R30Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361441
Start	39017956:39017956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365G>A
AA Mutation	p.Arg122His(p.R122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361441
Start	39017994:39017994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403C>T
AA Mutation	p.Leu135Phe(p.L135F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361441
Start	39017958:39017958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.367C>A
AA Mutation	p.Leu123Ile(p.L123I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361441
Start	39017942:39017942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361441
Start	39015661:39015661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773172607
CDS Mutation	c.84C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361441
Start	39017822:39017822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201615015
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000361441
Start	39015743:39015743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778502182
CDS Mutation	c.166C>T
AA Mutation	p.Arg56Ter(p.R56*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> APOBEC3C

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000361441
Start	39015743:39015743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778502182
CDS Mutation	c.166C>T
AA Mutation	p.Arg56Ter(p.R56*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript