Colon Cancer: Gene >> RARB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25501205:25501205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351G>T
AA Mutation	p.Gln117His(p.Q117H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25501282:25501282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428G>A
AA Mutation	p.Cys143Tyr(p.C143Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25501275:25501275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421C>G
AA Mutation	p.Gln141Glu(p.Q141E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25461221:25461221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.207G>T
AA Mutation	p.Glu69Asp(p.E69D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25580633:25580633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.718G>A
AA Mutation	p.Val240Met(p.V240M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25594660:25594660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759614000
CDS Mutation	c.1153C>T
AA Mutation	p.Arg385Cys(p.R385C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25569847:25569847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Leu187Phe(p.L187F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25593663:25593663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968A>G
AA Mutation	p.Asp323Gly(p.D323G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25593527:25593527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832A>G
AA Mutation	p.Thr278Ala(p.T278A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000383772
Start	25501269:25501269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.415C>T
AA Mutation	p.Arg139Ter(p.R139*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000383772
Start	25580564:25580564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649C>T
AA Mutation	p.Arg217Ter(p.R217*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RARB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25461201:25461201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187A>G
AA Mutation	p.Thr63Ala(p.T63A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000383772
Start	25593668:25593668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973G>T
AA Mutation	p.Glu325Ter(p.E325*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript