Colon Cancer: Gene >> JAZF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283928
Start	27832809:27832809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723G>A
AA Mutation	p.Met241Ile(p.M241I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283928
Start	27895351:27895351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254C>T
AA Mutation	p.Ser85Leu(p.S85L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283928
Start	27832924:27832924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608G>A
AA Mutation	p.Arg203His(p.R203H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000283928
Start	27895300:27895300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305G>A
AA Mutation	p.Arg102His(p.R102H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283928
Start	27840827:27840827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758412588
CDS Mutation	c.426G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283928
Start	27832953:27832953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148892911
CDS Mutation	c.579C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> JAZF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283928
Start	27895399:27895399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206C>T
AA Mutation	p.Ala69Val(p.A69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283928
Start	27895251:27895251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.354delC
AA Mutation	p.Ser119ProfsTer47(p.S119Pfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript