Colon Cancer: Gene >> ZNF185

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370268
Start	152920729:152920729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634G>A
AA Mutation	p.Ala212Thr(p.A212T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370268
Start	152931758:152931758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001C>T
AA Mutation	p.Pro334Leu(p.P334L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370268
Start	152932917:152932917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064C>T
AA Mutation	p.Thr355Met(p.T355M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370268
Start	152932910:152932910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201390993
CDS Mutation	c.1057G>A
AA Mutation	p.Gly353Arg(p.G353R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370268
Start	152945340:152945340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1282C>T
AA Mutation	p.Pro428Ser(p.P428S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370268
Start	152945383:152945383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1325C>A
AA Mutation	p.Pro442His(p.P442H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370268
Start	152932897:152932897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782288327
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370268
Start	152928653:152928653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.906A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000370268
Start	152922213:152922213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.694C>T
AA Mutation	p.Gln232Ter(p.Q232*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF185

No Mutation Annotation!