Colon Cancer: Gene >> FANCC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289081
Start	95107262:95107262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1337T>A
AA Mutation	p.Val446Glu(p.V446E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289081
Start	95249180:95249180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778951584
CDS Mutation	c.112G>A
AA Mutation	p.Val38Met(p.V38M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289081
Start	95101720:95101720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369636116
CDS Mutation	c.1664G>A
AA Mutation	p.Arg555Gln(p.R555Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000289081
Start	95135409:95135409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780G>T
AA Mutation	p.Lys260Asn(p.K260N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000289081
Start	95111630:95111630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371897078
CDS Mutation	c.1162G>A
AA Mutation	p.Gly388Arg(p.G388R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000289081
Start	95240705:95240705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289C>G
AA Mutation	p.Leu97Val(p.L97V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000289081
Start	95125109:95125109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973G>T
AA Mutation	p.Ala325Ser(p.A325S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000289081
Start	95247507:95247507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175A>G
AA Mutation	p.Thr59Ala(p.T59A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000289081
Start	95149990:95149990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619C>A
AA Mutation	p.His207Asn(p.H207N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289081
Start	95101818:95101818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1566C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000289081
Start	95107254:95107254(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1345delG
AA Mutation	p.Val449CysfsTer22(p.V449Cfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000289081
Start	95172137:95172138(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.355_356insAAATTTTAAATA
AA Mutation	p.Ser119delinsTer(p.S119delins*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FANCC

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000289081
Start	95107108:95107108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1491G>A
AA Mutation	p.Trp497Ter(p.W497*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript