Colon Cancer: Gene >> NR1D1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246672
Start	40097175:40097175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751801001
CDS Mutation	c.260C>T
AA Mutation	p.Ser87Leu(p.S87L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246672
Start	40095617:40095617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373443634
CDS Mutation	c.1075C>T
AA Mutation	p.Arg359Cys(p.R359C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246672
Start	40096482:40096482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.565C>T
AA Mutation	p.Arg189Cys(p.R189C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246672
Start	40097398:40097398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37G>A
AA Mutation	p.Val13Ile(p.V13I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000246672
Start	40093177:40093177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1751G>T
AA Mutation	p.Arg584Leu(p.R584L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000246672
Start	40093099:40093099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752175778
CDS Mutation	c.1829G>A
AA Mutation	p.Arg610Gln(p.R610Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000246672
Start	40096708:40096708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442G>A
AA Mutation	p.Ala148Thr(p.A148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000246672
Start	40095544:40095544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148G>A
AA Mutation	p.Ser383Asn(p.S383N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000246672
Start	40097172:40097172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766286236
CDS Mutation	c.263C>T
AA Mutation	p.Ser88Leu(p.S88L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246672
Start	40094045:40094045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1512C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246672
Start	40095786:40095786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150627138
CDS Mutation	c.906C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000246672
Start	40095081:40095081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1288C>T
AA Mutation	p.Arg430Ter(p.R430*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NR1D1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246672
Start	40093234:40093234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201684407
CDS Mutation	c.1694C>T
AA Mutation	p.Thr565Met(p.T565M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript