Colon Cancer: Gene >> NR2C1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333003
Start	95022354:95022354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1687A>G
AA Mutation	p.Thr563Ala(p.T563A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333003
Start	95058422:95058422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432T>A
AA Mutation	p.Asn144Lys(p.N144K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333003
Start	95025215:95025215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1572T>A
AA Mutation	p.Phe524Leu(p.F524L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333003
Start	95057579:95057579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.757T>G
AA Mutation	p.Ser253Ala(p.S253A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000333003
Start	95031376:95031376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1366A>G
AA Mutation	p.Asn456Asp(p.N456D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000333003
Start	95040575:95040575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1154C>A
AA Mutation	p.Pro385His(p.P385H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000333003
Start	95049232:95049232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.967G>A
AA Mutation	p.Ala323Thr(p.A323T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000333003
Start	95062642:95062642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144726031
CDS Mutation	c.151G>A
AA Mutation	p.Gly51Ser(p.G51S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333003
Start	95058407:95058407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.447T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333003
Start	95028427:95028427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1491C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000333003
Start	95049174:95049174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1025C>A
AA Mutation	p.Ser342Ter(p.S342*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NR2C1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333003
Start	95040584:95040584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1145C>T
AA Mutation	p.Ser382Phe(p.S382F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333003
Start	95049094:95049094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1105C>T
AA Mutation	p.Leu369Phe(p.L369F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript