Colon Cancer: Gene >> NFIC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000443272
Start	3452575:3452575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178C>T
AA Mutation	p.Ala393Val(p.A393V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000443272
Start	3381848:3381848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560121964
CDS Mutation	c.167C>A
AA Mutation	p.Ala56Glu(p.A56E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000443272
Start	3381844:3381844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.163C>T
AA Mutation	p.Arg55Cys(p.R55C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000443272
Start	3433589:3433589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757507471
CDS Mutation	c.706C>T
AA Mutation	p.Arg236Trp(p.R236W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000443272
Start	3381746:3381746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.65C>A
AA Mutation	p.Pro22His(p.P22H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000443272
Start	3435168:3435168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919A>T
AA Mutation	p.Thr307Ser(p.T307S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000443272
Start	3452665:3452665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771779620
CDS Mutation	c.1268C>T
AA Mutation	p.Pro423Leu(p.P423L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000443272
Start	3449074:3449074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1019C>T
AA Mutation	p.Pro340Leu(p.P340L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000443272
Start	3381732:3381732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.51C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000443272
Start	3433522:3433522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377664780
CDS Mutation	c.639G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000443272
Start	3452510:3452510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138179732
CDS Mutation	c.1113C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000443272
Start	3453855:3453855(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1367delC
AA Mutation	p.Pro456LeufsTer36(p.P456Lfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NFIC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000443272
Start	3434306:3434306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739T>G
AA Mutation	p.Phe247Val(p.F247V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript