Colon Cancer: Gene >> NR1H3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000441012
Start	47268661:47268661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1309C>T
AA Mutation	p.Pro437Ser(p.P437S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000441012
Start	47261596:47261596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565653980
CDS Mutation	c.758G>A
AA Mutation	p.Arg253His(p.R253H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000441012
Start	47260543:47260543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367C>T
AA Mutation	p.Arg123Cys(p.R123C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000441012
Start	47261577:47261577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778600458
CDS Mutation	c.739C>T
AA Mutation	p.Arg247Trp(p.R247W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000441012
Start	47261719:47261719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556085486
CDS Mutation	c.881C>T
AA Mutation	p.Ala294Val(p.A294V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000441012
Start	47268609:47268609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000441012
Start	47260429:47260429(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.257delA
AA Mutation	p.Lys86ArgfsTer28(p.K86Rfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000441012
Start	47261336:47261336(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.601delC
AA Mutation	p.Gln201LysfsTer13(p.Q201Kfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000441012
Start	47261317:47261318(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.582dupC
AA Mutation	p.Arg195GlnfsTer31(p.R195Qfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000441012
Start	47261335:47261336(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs779801455
CDS Mutation	c.601dupC
AA Mutation	p.Gln201ProfsTer25(p.Q201Pfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NR1H3

No Mutation Annotation!