Colon Cancer: Gene >> RXRA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000481739
Start	134401836:134401836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568762857
CDS Mutation	c.233C>T
AA Mutation	p.Ser78Leu(p.S78L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000481739
Start	134436553:134436553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1328G>A
AA Mutation	p.Gly443Glu(p.G443E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000481739
Start	134421688:134421688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793G>A
AA Mutation	p.Val265Ile(p.V265I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000481739
Start	134429128:134429128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931G>A
AA Mutation	p.Ala311Thr(p.A311T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000481739
Start	134429144:134429144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Arg316His(p.R316H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000481739
Start	134408194:134408194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325C>T
AA Mutation	p.Pro109Ser(p.P109S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000481739
Start	134417179:134417179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632G>A
AA Mutation	p.Arg211His(p.R211H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000481739
Start	134421800:134421800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905G>A
AA Mutation	p.Arg302Gln(p.R302Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000481739
Start	134436568:134436568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1343A>G
AA Mutation	p.Asp448Gly(p.D448G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000481739
Start	134436596:134436596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1371G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000481739
Start	134408169:134408169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571766607
CDS Mutation	c.300C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000481739
Start	134408181:134408181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143704037
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000481739
Start	134408194:134408194(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.331delC
AA Mutation	p.Leu111TrpfsTer57(p.L111Wfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000481739
Start	134401812:134401812(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.213delC
AA Mutation	p.Met72TrpfsTer27(p.M72Wfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RXRA

No Mutation Annotation!