Colon Cancer: Gene >> RCVRN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226193
Start	9905071:9905071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.110A>C
AA Mutation	p.Lys37Thr(p.K37T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226193
Start	9900999:9900999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483G>T
AA Mutation	p.Lys161Asn(p.K161N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226193
Start	9904979:9904979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202C>T
AA Mutation	p.His68Tyr(p.H68Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226193
Start	9904898:9904898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117017774
CDS Mutation	c.283G>A
AA Mutation	p.Ala95Thr(p.A95T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000226193
Start	9901025:9901025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754840876
CDS Mutation	c.457G>A
AA Mutation	p.Glu153Lys(p.E153K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226193
Start	9905022:9905022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226193
Start	9904923:9904923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764982768
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226193
Start	9901053:9901053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745310288
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226193
Start	9904962:9904962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226193
Start	9898122:9898122(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.576delA
AA Mutation	p.Val193Ter(p.V193*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RCVRN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226193
Start	9898183:9898183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515T>G
AA Mutation	p.Phe172Cys(p.F172C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript