Colon Cancer: Gene >> NUSAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000559596
Start	41365555:41365555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Cys(p.R272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000559596
Start	41365520:41365520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.779G>C
AA Mutation	p.Ser260Thr(p.S260T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000559596
Start	41349172:41349172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NUSAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000559596
Start	41351029:41351029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348C>A
AA Mutation	p.Phe116Leu(p.F116L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript