Colon Cancer: Gene >> HMGCR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287936
Start	75359269:75359269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2257G>T
AA Mutation	p.Ala753Ser(p.A753S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287936
Start	75344306:75344306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339C>A
AA Mutation	p.Phe113Leu(p.F113L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287936
Start	75350332:75350332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738A>C
AA Mutation	p.Glu246Asp(p.E246D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287936
Start	75355510:75355510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1868A>C
AA Mutation	p.Asp623Ala(p.D623A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287936
Start	75342714:75342714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109T>C
AA Mutation	p.Phe37Leu(p.F37L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287936
Start	75347253:75347253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500C>T
AA Mutation	p.Thr167Met(p.T167M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287936
Start	75355410:75355410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1768C>T
AA Mutation	p.Arg590Cys(p.R590C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287936
Start	75355142:75355142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1650A>T
AA Mutation	p.Glu550Asp(p.E550D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287936
Start	75351303:75351303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371909330
CDS Mutation	c.1177C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287936
Start	75345646:75345646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287936
Start	75360062:75360062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748889378
CDS Mutation	c.2535C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287936
Start	75354685:75354685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1551T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HMGCR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287936
Start	75343938:75343938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372565038
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287936
Start	75360046:75360046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755619444
CDS Mutation	c.2519G>A
AA Mutation	p.Arg840Gln(p.R840Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287936
Start	75351226:75351226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1100A>C
AA Mutation	p.Asn367Thr(p.N367T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000287936
Start	75344316:75344316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>T
AA Mutation	p.Glu117Ter(p.E117*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript