Colon Cancer: Gene >> NFIB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380959
Start	14120463:14120463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1222C>T
AA Mutation	p.Pro408Ser(p.P408S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380959
Start	14125641:14125641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1051G>A
AA Mutation	p.Ala351Thr(p.A351T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380959
Start	14125697:14125697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995C>T
AA Mutation	p.Ser332Phe(p.S332F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380959
Start	14146731:14146731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.883T>C
AA Mutation	p.Ser295Pro(p.S295P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380959
Start	14179742:14179742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601G>A
AA Mutation	p.Ala201Thr(p.A201T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380959
Start	14307196:14307196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Asp119Asn(p.D119N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380959
Start	14307435:14307435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116G>A
AA Mutation	p.Arg39His(p.R39H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380959
Start	14150189:14150189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.762C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380959
Start	14307385:14307386(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.165_166delAG
AA Mutation	p.Arg55SerfsTer5(p.R55Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380959
Start	14307175:14307178(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.373_376delGACA
AA Mutation	p.Asp125LysfsTer7(p.D125Kfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000380959
Start	14150224:14150224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727G>T
AA Mutation	p.Glu243Ter(p.E243*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000380959
Start	14307167:14307167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.384G>A
AA Mutation	p.Trp128Ter(p.W128*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000380959
Start	14307187:14307187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Ter(p.R122*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NFIB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380959
Start	14120604:14120604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081C>G
AA Mutation	p.Pro361Ala(p.P361A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380959
Start	14307165:14307165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386G>A
AA Mutation	p.Arg129His(p.R129H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380959
Start	14307499:14307499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52G>A
AA Mutation	p.Glu18Lys(p.E18K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380959
Start	14307163:14307163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.388C>G
AA Mutation	p.Leu130Val(p.L130V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript