Colon Cancer: Gene >> NOC3L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371361
Start	94340322:94340322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1734G>T
AA Mutation	p.Leu578Phe(p.L578F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371361
Start	94344928:94344928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1395G>T
AA Mutation	p.Lys465Asn(p.K465N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371361
Start	94349349:94349349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1158G>T
AA Mutation	p.Lys386Asn(p.K386N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371361
Start	94354989:94354989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670G>A
AA Mutation	p.Ala224Thr(p.A224T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371361
Start	94346478:94346478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336A>C
AA Mutation	p.Lys446Gln(p.K446Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371361
Start	94357296:94357296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763109129
CDS Mutation	c.386G>A
AA Mutation	p.Arg129His(p.R129H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371361
Start	94334681:94334681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2227G>A
AA Mutation	p.Glu743Lys(p.E743K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371361
Start	94358187:94358187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371361
Start	94357220:94357220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371361
Start	94361735:94361735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371361
Start	94346540:94346540(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs780830188
CDS Mutation	c.1274delT
AA Mutation	p.Leu425TyrfsTer3(p.L425Yfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371361
Start	94346547:94346547(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1267delA
AA Mutation	p.Thr423HisfsTer5(p.T423Hfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371361
Start	94353049:94353049(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.705delA
AA Mutation	p.Lys235AsnfsTer2(p.K235Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000371361
Start	94352394:94352394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868G>T
AA Mutation	p.Glu290Ter(p.E290*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NOC3L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371361
Start	94350217:94350217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142493625
CDS Mutation	c.1024G>A
AA Mutation	p.Ala342Thr(p.A342T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371361
Start	94352908:94352908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.846A>C
AA Mutation	p.Glu282Asp(p.E282D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371361
Start	94355032:94355032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.627G>T
AA Mutation	p.Lys209Asn(p.K209N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371361
Start	94358114:94358114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.319G>T
AA Mutation	p.Val107Leu(p.V107L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371361
Start	94334204:94334204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2376G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000371361
Start	94353042:94353042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712G>T
AA Mutation	p.Glu238Ter(p.E238*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript