Colon Cancer: Gene >> SOD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000538183
Start	159685010:159685010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143582231
CDS Mutation	c.367C>T
AA Mutation	p.Arg123Cys(p.R123C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000538183
Start	159682581:159682581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581A>C
AA Mutation	p.Lys194Thr(p.K194T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000538183
Start	159684968:159684968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.409G>A
AA Mutation	p.Ala137Thr(p.A137T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000538183
Start	159682600:159682600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562G>A
AA Mutation	p.Ala188Thr(p.A188T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000538183
Start	159688210:159688210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.259G>A
AA Mutation	p.Ala87Thr(p.A87T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000538183
Start	159684876:159684876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501G>T
AA Mutation	p.Gln167His(p.Q167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000538183
Start	159684970:159684970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372074075
CDS Mutation	c.407C>T
AA Mutation	p.Thr136Met(p.T136M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000538183
Start	159688240:159688240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229G>A
AA Mutation	p.Asp77Asn(p.D77N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000538183
Start	159684957:159684957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.420T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SOD2

No Mutation Annotation!