Colon Cancer: Gene >> SAPCD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409687
Start	137064765:137064765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1079G>A
AA Mutation	p.Arg360His(p.R360H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409687
Start	137066359:137066359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587G>C
AA Mutation	p.Arg196Thr(p.R196T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409687
Start	137065602:137065602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751542754
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Trp(p.R251W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000409687
Start	137066318:137066318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567953393
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Cys(p.R210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409687
Start	137064971:137064971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SAPCD2

No Mutation Annotation!