Colon Cancer: Gene >> RORB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74662550:74662550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770337953
CDS Mutation	c.869G>A
AA Mutation	p.Arg290Gln(p.R290Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74665518:74665518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956G>C
AA Mutation	p.Cys319Ser(p.C319S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74662496:74662496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815A>G
AA Mutation	p.Gln272Arg(p.Q272R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74634710:74634710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206A>G
AA Mutation	p.Asn69Ser(p.N69S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74634707:74634707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779534868
CDS Mutation	c.203C>T
AA Mutation	p.Thr68Met(p.T68M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74630345:74630345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104T>C
AA Mutation	p.Val35Ala(p.V35A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74642528:74642528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383C>T
AA Mutation	p.Ala128Val(p.A128V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74671848:74671848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1204G>T
AA Mutation	p.Ala402Ser(p.A402S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74642614:74642614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Val157Ile(p.V157I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74642657:74642657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747948403
CDS Mutation	c.512C>T
AA Mutation	p.Ser171Phe(p.S171F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74662549:74662549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Trp(p.R290W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74642450:74642450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305A>T
AA Mutation	p.Asp102Val(p.D102V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000396204
Start	74634675:74634675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171C>G
AA Mutation	p.Cys57Trp(p.C57W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396204
Start	74642607:74642607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573233356
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396204
Start	74634708:74634708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396204
Start	74667807:74667807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1050G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396204
Start	74642613:74642613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396204
Start	74667867:74667867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000396204
Start	74642707:74642707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562C>T
AA Mutation	p.Gln188Ter(p.Q188*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RORB

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396204
Start	74642661:74642661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000376896
Start	74497980:74497980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4C>T
AA Mutation	p.Arg2Ter(p.R2*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript