Colon Cancer: Gene >> NEIL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355059
Start	75348921:75348921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16G>A
AA Mutation	p.Glu6Lys(p.E6K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355059
Start	75349020:75349020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.115C>T
AA Mutation	p.Pro39Ser(p.P39S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355059
Start	75349006:75349006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.101G>A
AA Mutation	p.Arg34His(p.R34H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355059
Start	75353763:75353763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.743G>A
AA Mutation	p.Ser248Asn(p.S248N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355059
Start	75352151:75352151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475C>T
AA Mutation	p.Arg159Trp(p.R159W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355059
Start	75354804:75354804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376283006
CDS Mutation	c.1088G>A
AA Mutation	p.Arg363Gln(p.R363Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355059
Start	75349262:75349262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763707906
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355059
Start	75349157:75349157(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.255delT
AA Mutation	p.Gln86SerfsTer67(p.Q86Sfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355059
Start	75352333:75352333(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.570delC
AA Mutation	p.Phe191LeufsTer20(p.F191Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NEIL1

No Mutation Annotation!