Colon Cancer: Gene >> NFIL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297689
Start	91410494:91410494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241C>T
AA Mutation	p.Arg81Trp(p.R81W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297689
Start	91410357:91410357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.378T>G
AA Mutation	p.Phe126Leu(p.F126L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297689
Start	91409405:91409405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1330G>A
AA Mutation	p.Val444Ile(p.V444I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297689
Start	91410524:91410524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.211A>G
AA Mutation	p.Lys71Glu(p.K71E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297689
Start	91410637:91410637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780645794
CDS Mutation	c.98C>T
AA Mutation	p.Thr33Met(p.T33M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297689
Start	91410463:91410463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272G>A
AA Mutation	p.Arg91His(p.R91H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000297689
Start	91409406:91409406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329G>T
AA Mutation	p.Glu443Asp(p.E443D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000297689
Start	91410656:91410656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.79G>A
AA Mutation	p.Val27Ile(p.V27I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000297689
Start	91409615:91409615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773631235
CDS Mutation	c.1120G>A
AA Mutation	p.Val374Ile(p.V374I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297689
Start	91410264:91410264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297689
Start	91410105:91410105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297689
Start	91409691:91409691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141662610
CDS Mutation	c.1044G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NFIL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297689
Start	91410394:91410394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.341C>T
AA Mutation	p.Thr114Ile(p.T114I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297689
Start	91409645:91409645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34945709
CDS Mutation	c.1090G>A
AA Mutation	p.Glu364Lys(p.E364K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000297689
Start	91409531:91409531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1204G>T
AA Mutation	p.Glu402Ter(p.E402*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript