Colon Cancer: Gene >> ZNF202

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336139
Start	123728237:123728237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728C>T
AA Mutation	p.Ala243Val(p.A243V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336139
Start	123729668:123729668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201276058
CDS Mutation	c.560C>T
AA Mutation	p.Pro187Leu(p.P187L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336139
Start	123726155:123726155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1789G>A
AA Mutation	p.Glu597Lys(p.E597K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336139
Start	123726835:123726835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109T>G
AA Mutation	p.Phe370Cys(p.F370C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336139
Start	123730682:123730682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.207A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336139
Start	123726267:123726267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774625759
CDS Mutation	c.1677C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336139
Start	123729808:123729808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760045159
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336139
Start	123730547:123730547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000336139
Start	123726386:123726386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1558C>T
AA Mutation	p.Gln520Ter(p.Q520*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF202

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336139
Start	123730855:123730855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34C>A
AA Mutation	p.Leu12Ile(p.L12I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000336139
Start	123729759:123729759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.469G>T
AA Mutation	p.Glu157Ter(p.E157*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript