Colon Cancer: Gene >> RELB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221452
Start	45011971:45011971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376021184
CDS Mutation	c.199G>A
AA Mutation	p.Gly67Ser(p.G67S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221452
Start	45037509:45037509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1459G>A
AA Mutation	p.Asp487Asn(p.D487N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221452
Start	45037491:45037491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374272785
CDS Mutation	c.1441G>A
AA Mutation	p.Gly481Arg(p.G481R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221452
Start	45025388:45025388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755747339
CDS Mutation	c.722G>A
AA Mutation	p.Arg241Gln(p.R241Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221452
Start	45028921:45028921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920G>A
AA Mutation	p.Arg307Gln(p.R307Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000221452
Start	45025674:45025674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747326911
CDS Mutation	c.823C>T
AA Mutation	p.Arg275Trp(p.R275W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000221452
Start	45037737:45037737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770578374
CDS Mutation	c.1687C>T
AA Mutation	p.Arg563Cys(p.R563C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221452
Start	45025718:45025718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570531651
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221452
Start	45011997:45011997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762605645
CDS Mutation	c.225G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221452
Start	45011979:45011979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.207C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221452
Start	45037460:45037460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764829693
CDS Mutation	c.1410C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221452
Start	45034491:45034491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369885274
CDS Mutation	c.1317G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RELB

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221452
Start	45025697:45025697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.846C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221452
Start	45034284:45034284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368632431
CDS Mutation	c.1248C>T
Mutation Classification	Silent
Feature Type	Transcript