Colon Cancer: Gene >> HAO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378789
Start	7914195:7914195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778551661
CDS Mutation	c.514C>T
AA Mutation	p.Arg172Cys(p.R172C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378789
Start	7914297:7914297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412G>A
AA Mutation	p.Glu138Lys(p.E138K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378789
Start	7885726:7885726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751134577
CDS Mutation	c.952G>A
AA Mutation	p.Val318Ile(p.V318I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378789
Start	7914276:7914276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200785017
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Trp(p.R145W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378789
Start	7934522:7934522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768341358
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378789
Start	7934505:7934505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746154151
CDS Mutation	c.268G>A
AA Mutation	p.Gly90Ser(p.G90S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378789
Start	7914173:7914173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536C>T
AA Mutation	p.Pro179Leu(p.P179L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000378789
Start	7883628:7883628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078G>A
AA Mutation	p.Val360Met(p.V360M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378789
Start	7895199:7895199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.747A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378789
Start	7914352:7914352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373499154
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378789
Start	7906269:7906269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HAO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378789
Start	7914276:7914276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200785017
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Trp(p.R145W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378789
Start	7906271:7906271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780735238
CDS Mutation	c.604G>A
AA Mutation	p.Asp202Asn(p.D202N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378789
Start	7906196:7906196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.679A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378789
Start	7885542:7885542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1021C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000378789
Start	7906330:7906330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.546-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript