Colon Cancer: Gene >> RNF123

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49697399:49697399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284T>C
AA Mutation	p.Val95Ala(p.V95A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49712616:49712616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2634G>T
AA Mutation	p.Lys878Asn(p.K878N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49703496:49703496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1820G>T
AA Mutation	p.Gly607Val(p.G607V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49701863:49701863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1448G>A
AA Mutation	p.Arg483Gln(p.R483Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49720636:49720636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754168663
CDS Mutation	c.3626G>A
AA Mutation	p.Arg1209His(p.R1209H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49713917:49713917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368723431
CDS Mutation	c.2845G>A
AA Mutation	p.Ala949Thr(p.A949T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49701513:49701513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751933046
CDS Mutation	c.1300G>A
AA Mutation	p.Val434Ile(p.V434I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000327697
Start	49702403:49702403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1627G>A
AA Mutation	p.Gly543Arg(p.G543R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49699674:49699674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372770015
CDS Mutation	c.886C>T
AA Mutation	p.Arg296Trp(p.R296W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49701541:49701541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770811607
CDS Mutation	c.1328G>A
AA Mutation	p.Arg443His(p.R443H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49715912:49715912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3241C>A
AA Mutation	p.Leu1081Met(p.L1081M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49698500:49698500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544A>G
AA Mutation	p.Asn182Asp(p.N182D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49700648:49700648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369371695
CDS Mutation	c.1216C>T
AA Mutation	p.Arg406Trp(p.R406W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49716441:49716441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3464T>C
AA Mutation	p.Ile1155Thr(p.I1155T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49720606:49720606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3596G>A
AA Mutation	p.Gly1199Asp(p.G1199D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49721249:49721249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3889T>C
AA Mutation	p.Ser1297Pro(p.S1297P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49720629:49720629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762516169
CDS Mutation	c.3619C>T
AA Mutation	p.Arg1207Trp(p.R1207W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49706049:49706049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376679342
CDS Mutation	c.2372G>A
AA Mutation	p.Arg791His(p.R791H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000327697
Start	49713912:49713912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150915433
CDS Mutation	c.2840G>A
AA Mutation	p.Arg947His(p.R947H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49720821:49720821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3665A>G
AA Mutation	p.Asp1222Gly(p.D1222G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49704709:49704709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1912A>G
AA Mutation	p.Met638Val(p.M638V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327697
Start	49705154:49705154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2130G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327697
Start	49702659:49702659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1656G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327697
Start	49699538:49699538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327697
Start	49712535:49712535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770060614
CDS Mutation	c.2553C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327697
Start	49721200:49721200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3840G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RNF123

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327697
Start	49700317:49700317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075C>T
AA Mutation	p.His359Tyr(p.H359Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000327697
Start	49699105:49699105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746387724
CDS Mutation	c.764G>A
AA Mutation	p.Arg255His(p.R255H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327697
Start	49701873:49701873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758308937
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327697
Start	49704696:49704696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1899C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327697
Start	49702401:49702401(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1629+1delG
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript