Colon Cancer: Gene >> RNF20

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000389120
Start	101546964:101546964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753765875
CDS Mutation	c.892C>T
AA Mutation	p.Arg298Trp(p.R298W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101560921:101560921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769326539
CDS Mutation	c.2503C>T
AA Mutation	p.Arg835Cys(p.R835C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101550616:101550616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368721473
CDS Mutation	c.1103G>A
AA Mutation	p.Arg368Gln(p.R368Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101551771:101551771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1360A>G
AA Mutation	p.Met454Val(p.M454V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101540834:101540834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487G>A
AA Mutation	p.Ala163Thr(p.A163T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101562340:101562340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757082884
CDS Mutation	c.2846G>A
AA Mutation	p.Arg949His(p.R949H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101547474:101547474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761717076
CDS Mutation	c.1048C>T
AA Mutation	p.Arg350Trp(p.R350W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101550681:101550681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755745298
CDS Mutation	c.1168G>A
AA Mutation	p.Val390Ile(p.V390I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101550669:101550669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1156T>C
AA Mutation	p.Ser386Pro(p.S386P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101540505:101540505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313C>T
AA Mutation	p.Arg105Cys(p.R105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000389120
Start	101552563:101552563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142811207
CDS Mutation	c.1711C>T
AA Mutation	p.Arg571Ter(p.R571*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000389120
Start	101552557:101552557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535787053
CDS Mutation	c.1705C>T
AA Mutation	p.Arg569Ter(p.R569*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000389120
Start	101546931:101546931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759230038
CDS Mutation	c.859C>T
AA Mutation	p.Arg287Ter(p.R287*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000389120
Start	101554107:101554107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2019+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RNF20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101552497:101552497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645G>A
AA Mutation	p.Ala549Thr(p.A549T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101560807:101560807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2389G>A
AA Mutation	p.Ala797Thr(p.A797T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101561223:101561223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776618752
CDS Mutation	c.2642G>A
AA Mutation	p.Arg881Gln(p.R881Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389120
Start	101540315:101540315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242G>A
AA Mutation	p.Arg81Gln(p.R81Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript