Colon Cancer: Gene >> PROM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95276996:95276996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535604152
CDS Mutation	c.707C>T
AA Mutation	p.Ala236Val(p.A236V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95275946:95275946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376702791
CDS Mutation	c.311C>T
AA Mutation	p.Ala104Val(p.A104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95284984:95284984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553459907
CDS Mutation	c.1744C>T
AA Mutation	p.Arg582Trp(p.R582W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95287434:95287434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2214C>A
AA Mutation	p.Phe738Leu(p.F738L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95281268:95281268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1454C>T
AA Mutation	p.Ala485Val(p.A485V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95275973:95275973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201610848
CDS Mutation	c.338C>T
AA Mutation	p.Ala113Val(p.A113V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95281310:95281310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1496G>T
AA Mutation	p.Gly499Val(p.G499V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95274791:95274791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758232721
CDS Mutation	c.206G>A
AA Mutation	p.Arg69His(p.R69H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95276324:95276324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595G>A
AA Mutation	p.Gly199Ser(p.G199S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95277976:95277976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1022A>C
AA Mutation	p.Glu341Ala(p.E341A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317620
Start	95282196:95282196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750880470
CDS Mutation	c.1698C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317620
Start	95279884:95279884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749141766
CDS Mutation	c.1314C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317620
Start	95279860:95279860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145337849
CDS Mutation	c.1290C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317620
Start	95279971:95279971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140258551
CDS Mutation	c.1401C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317620
Start	95274690:95274690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776099688
CDS Mutation	c.105G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317620
Start	95274727:95274727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317620
Start	95276088:95276088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372178611
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317620
Start	95281969:95281969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769412772
CDS Mutation	c.1596G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000317620
Start	95279998:95279998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200030602
CDS Mutation	c.1427+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PROM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95281318:95281318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1504G>A
AA Mutation	p.Val502Met(p.V502M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317620
Start	95288539:95288539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2391C>G
AA Mutation	p.Ile797Met(p.I797M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317620
Start	95275971:95275971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544194496
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript