Colon Cancer: Gene >> RUVBL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322623
Start	128104816:128104816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470T>A
AA Mutation	p.Val157Glu(p.V157E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322623
Start	128100605:128100605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743C>T
AA Mutation	p.Ala248Val(p.A248V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322623
Start	128112900:128112900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Cys(p.R117C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322623
Start	128101611:128101611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551G>A
AA Mutation	p.Arg184Gln(p.R184Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322623
Start	128104854:128104854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432G>T
AA Mutation	p.Glu144Asp(p.E144D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322623
Start	128104796:128104796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490G>A
AA Mutation	p.Ala164Thr(p.A164T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000322623
Start	128087768:128087768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057G>A
AA Mutation	p.Asp353Asn(p.D353N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000322623
Start	128081330:128081330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291G>A
AA Mutation	p.Glu431Lys(p.E431K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RUVBL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322623
Start	128081330:128081330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291G>A
AA Mutation	p.Glu431Lys(p.E431K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322623
Start	128104901:128104901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772341250
CDS Mutation	c.385G>A
AA Mutation	p.Glu129Lys(p.E129K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript