Colon Cancer: Gene >> RNASEH2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221486
Start	12807322:12807322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316C>T
AA Mutation	p.Leu106Phe(p.L106F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221486
Start	12807492:12807492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397G>A
AA Mutation	p.Val133Met(p.V133M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221486
Start	12810114:12810114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757486362
CDS Mutation	c.455G>A
AA Mutation	p.Arg152Gln(p.R152Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221486
Start	12813114:12813114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531859310
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RNASEH2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221486
Start	12807492:12807492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397G>A
AA Mutation	p.Val133Met(p.V133M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221486
Start	12807273:12807273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765310821
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000221486
Start	12807418:12807418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.324-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript