Colon Cancer: Gene >> NR5A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373588
Start	124500710:124500710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250C>T
AA Mutation	p.Arg84Cys(p.R84C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373588
Start	124491200:124491200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780199277
CDS Mutation	c.1019C>T
AA Mutation	p.Ala340Val(p.A340V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373588
Start	124503139:124503139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184C>T
AA Mutation	p.Arg62Cys(p.R62C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373588
Start	124482949:124482949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1195G>A
AA Mutation	p.Ala399Thr(p.A399T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373588
Start	124500700:124500700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260G>A
AA Mutation	p.Arg87His(p.R87H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373588
Start	124500709:124500709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375469069
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373588
Start	124500330:124500330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779933883
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373588
Start	124500577:124500578(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.382dupG
AA Mutation	p.Val128GlyfsTer21(p.V128Gfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NR5A1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373588
Start	124500228:124500228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.732C>A
Mutation Classification	Silent
Feature Type	Transcript