Colon Cancer: Gene >> NEIL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264596
Start	177351541:177351541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1031G>A
AA Mutation	p.Arg344Lys(p.R344K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264596
Start	177353709:177353709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1441A>G
AA Mutation	p.Asn481Asp(p.N481D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264596
Start	177360535:177360535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1493G>A
AA Mutation	p.Arg498His(p.R498H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264596
Start	177322526:177322526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224G>A
AA Mutation	p.Gly75Asp(p.G75D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264596
Start	177360574:177360574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1532A>G
AA Mutation	p.Asn511Ser(p.N511S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264596
Start	177341566:177341566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762418261
CDS Mutation	c.793C>T
AA Mutation	p.Arg265Cys(p.R265C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264596
Start	177353609:177353609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566894700
CDS Mutation	c.1341A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264596
Start	177362387:177362387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1734G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264596
Start	177335697:177335697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532020443
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NEIL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264596
Start	177335799:177335799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390C>A
AA Mutation	p.Phe130Leu(p.F130L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript