Colon Cancer: Gene >> UTP23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309822
Start	116766764:116766764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161T>C
AA Mutation	p.Met54Thr(p.M54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309822
Start	116771461:116771461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369G>T
AA Mutation	p.Gln123His(p.Q123H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309822
Start	116771786:116771786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752871869
CDS Mutation	c.694C>T
AA Mutation	p.Arg232Trp(p.R232W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309822
Start	116771492:116771492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400G>C
AA Mutation	p.Gly134Arg(p.G134R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309822
Start	116771794:116771794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702A>T
AA Mutation	p.Arg234Ser(p.R234S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309822
Start	116771797:116771797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000309822
Start	116771609:116771609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>T
AA Mutation	p.Glu173Ter(p.E173*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000309822
Start	116770244:116770245(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.241_242insAATAGTCGATTTTT
AA Mutation	p.Leu81GlnfsTer2(p.L81Qfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UTP23

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309822
Start	116771593:116771593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000309822
Start	116766627:116766641(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.26_40delCCAAGAAGCATCTTG
AA Mutation	p.Ala9_Leu13del(p.A9_L13del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript