Colon Cancer: Gene >> TXNRD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000525566
Start	104325401:104325401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1280A>T
AA Mutation	p.Glu427Val(p.E427V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000525566
Start	104321095:104321095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.994G>T
AA Mutation	p.Asp332Tyr(p.D332Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000525566
Start	104319495:104319495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899A>C
AA Mutation	p.Lys300Thr(p.K300T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000525566
Start	104348411:104348411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940G>A
AA Mutation	p.Cys647Tyr(p.C647Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000525566
Start	104319486:104319486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890G>A
AA Mutation	p.Gly297Asp(p.G297D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000525566
Start	104258038:104258038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263C>A
AA Mutation	p.Ser88Tyr(p.S88Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000525566
Start	104318982:104318982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189358801
CDS Mutation	c.800G>A
AA Mutation	p.Arg267Gln(p.R267Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000525566
Start	104319496:104319496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900A>C
AA Mutation	p.Lys300Asn(p.K300N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000525566
Start	104319552:104319552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956G>A
AA Mutation	p.Gly319Asp(p.G319D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000525566
Start	104321304:104321304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547545865
CDS Mutation	c.1203C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000525566
Start	104289022:104289022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000525566
Start	104319056:104319056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TXNRD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000525566
Start	104326381:104326381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1343G>A
AA Mutation	p.Arg448Lys(p.R448K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000525566
Start	104251667:104251667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769989720
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Cys(p.R78C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000525566
Start	104315890:104315890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724G>T
AA Mutation	p.Glu242Ter(p.E242*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript