Colon Cancer: Gene >> RFPL4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000434937
Start	55762729:55762729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777645016
CDS Mutation	c.418G>A
AA Mutation	p.Val140Ile(p.V140I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000434937
Start	55763095:55763095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.784G>A
AA Mutation	p.Asp262Asn(p.D262N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000434937
Start	55762745:55762745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.434G>A
AA Mutation	p.Arg145His(p.R145H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000434937
Start	55762810:55762810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752204786
CDS Mutation	c.499G>A
AA Mutation	p.Val167Met(p.V167M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000434937
Start	55763063:55763063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775264890
CDS Mutation	c.752G>A
AA Mutation	p.Arg251His(p.R251H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000434937
Start	55761904:55761904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104T>C
AA Mutation	p.Leu35Pro(p.L35P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000434937
Start	55762723:55762723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412C>A
AA Mutation	p.Leu138Met(p.L138M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RFPL4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000434937
Start	55762618:55762618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307G>C
AA Mutation	p.Asp103His(p.D103H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000434937
Start	55763061:55763061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200485809
CDS Mutation	c.750G>T
AA Mutation	p.Trp250Cys(p.W250C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript