Colon Cancer: Gene >> THAP11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303596
Start	67843330:67843330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776G>A
AA Mutation	p.Arg259His(p.R259H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303596
Start	67842728:67842728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303596
Start	67843094:67843094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303596
Start	67843251:67843251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.700delG
AA Mutation	p.Glu234LysfsTer28(p.E234Kfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303596
Start	67843379:67843382(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.827_830delAAGA
AA Mutation	p.Lys276ArgfsTer2(p.K276Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> THAP11

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303596
Start	67843097:67843097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543T>C
Mutation Classification	Silent
Feature Type	Transcript