Colon Cancer: Gene >> RNF220

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355387
Start	44636132:44636132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1096G>A
AA Mutation	p.Ala366Thr(p.A366T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355387
Start	44649925:44649925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1597G>A
AA Mutation	p.Val533Met(p.V533M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355387
Start	44649898:44649898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1570C>T
AA Mutation	p.Pro524Ser(p.P524S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355387
Start	44635565:44635565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775421926
CDS Mutation	c.970C>T
AA Mutation	p.Arg324Trp(p.R324W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355387
Start	44626308:44626308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.816G>C
AA Mutation	p.Leu272Phe(p.L272F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355387
Start	44412710:44412710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613C>T
AA Mutation	p.Arg205Trp(p.R205W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355387
Start	44412507:44412507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764633164
CDS Mutation	c.410C>T
AA Mutation	p.Thr137Met(p.T137M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355387
Start	44626344:44626344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369684385
CDS Mutation	c.852G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355387
Start	44614289:44614289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000355387
Start	44412532:44412532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>A
AA Mutation	p.Cys145Ter(p.C145*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000355387
Start	44412233:44412233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136C>T
AA Mutation	p.Arg46Ter(p.R46*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RNF220

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355387
Start	44412447:44412447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350T>G
AA Mutation	p.Val117Gly(p.V117G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript