Colon Cancer: Gene >> NUMB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355058
Start	73279346:73279346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149035382
CDS Mutation	c.1175G>A
AA Mutation	p.Arg392His(p.R392H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355058
Start	73292751:73292751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433A>G
AA Mutation	p.Met145Val(p.M145V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355058
Start	73276709:73276709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1825G>T
AA Mutation	p.Gly609Cys(p.G609C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355058
Start	73276729:73276729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1805G>T
AA Mutation	p.Arg602Met(p.R602M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355058
Start	73276960:73276960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1574C>A
AA Mutation	p.Pro525His(p.P525H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355058
Start	73284324:73284324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706G>A
AA Mutation	p.Ala236Thr(p.A236T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355058
Start	73284247:73284247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.783C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000355058
Start	73355664:73355664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88G>T
AA Mutation	p.Glu30Ter(p.E30*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000355058
Start	73297253:73297253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267G>A
AA Mutation	p.Trp89Ter(p.W89*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NUMB

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355058
Start	73287288:73287288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.477C>T
Mutation Classification	Silent
Feature Type	Transcript