Colon Cancer: Gene >> FOXN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48375378:48375378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377347494
CDS Mutation	c.1231C>T
AA Mutation	p.Arg411Cys(p.R411C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48346494:48346494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.280C>T
AA Mutation	p.Pro94Ser(p.P94S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48375259:48375259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1112C>G
AA Mutation	p.Pro371Arg(p.P371R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48374929:48374929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.782C>A
AA Mutation	p.Pro261His(p.P261H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48346530:48346530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316A>C
AA Mutation	p.Lys106Gln(p.K106Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48375019:48375019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872C>A
AA Mutation	p.Ser291Tyr(p.S291Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48346717:48346717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763008415
CDS Mutation	c.503A>C
AA Mutation	p.Lys168Thr(p.K168T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48375432:48375432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143561178
CDS Mutation	c.1285C>T
AA Mutation	p.Arg429Trp(p.R429W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48346276:48346276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62T>A
AA Mutation	p.Ile21Asn(p.I21N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340553
Start	48375281:48375281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000340553
Start	48346695:48346695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481C>T
AA Mutation	p.Arg161Ter(p.R161*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340553
Start	48375265:48375266(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1123dupA
AA Mutation	p.Ile375AsnfsTer3(p.I375Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FOXN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48346628:48346628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414T>G
AA Mutation	p.Ile138Met(p.I138M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48362648:48362648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.644C>A
AA Mutation	p.Ser215Tyr(p.S215Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340553
Start	48374958:48374958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811A>C
AA Mutation	p.Lys271Gln(p.K271Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript