Colon Cancer: Gene >> UGT1A10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344644
Start	233637165:233637165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643G>A
AA Mutation	p.Glu215Lys(p.E215K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344644
Start	233636888:233636888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767585841
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344644
Start	233636963:233636963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766629881
CDS Mutation	c.441G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344644
Start	233637098:233637098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344644
Start	233637030:233637031(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.512dupG
AA Mutation	p.Ile172AsnfsTer7(p.I172Nfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> UGT1A10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344644
Start	233636944:233636944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422C>A
AA Mutation	p.Ser141Tyr(p.S141Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344644
Start	233636880:233636880(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.364delT
AA Mutation	p.Ser122ArgfsTer12(p.S122Rfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript