Colon Cancer: Gene >> GLRX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331244
Start	130160983:130160983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.464A>C
AA Mutation	p.Gln155Pro(p.Q155P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331244
Start	130179381:130179381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997G>A
AA Mutation	p.Gly333Arg(p.G333R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331244
Start	130160860:130160860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775786978
CDS Mutation	c.341G>A
AA Mutation	p.Arg114Gln(p.R114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331244
Start	130179376:130179376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992T>C
AA Mutation	p.Leu331Pro(p.L331P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331244
Start	130174886:130174886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751236022
CDS Mutation	c.844G>A
AA Mutation	p.Asp282Asn(p.D282N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331244
Start	130145314:130145314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753162172
CDS Mutation	c.196G>A
AA Mutation	p.Val66Met(p.V66M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331244
Start	130145269:130145269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188360612
CDS Mutation	c.151G>A
AA Mutation	p.Glu51Lys(p.E51K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331244
Start	130174872:130174872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.830A>G
AA Mutation	p.Glu277Gly(p.E277G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331244
Start	130175020:130175020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.888C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000331244
Start	130145293:130145293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175G>T
AA Mutation	p.Glu59Ter(p.E59*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GLRX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331244
Start	130160994:130160994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.475T>C
AA Mutation	p.Cys159Arg(p.C159R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000331244
Start	130166937:130166937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670G>T
AA Mutation	p.Glu224Ter(p.E224*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript