Colon Cancer: Gene >> RBM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66639869:66639869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765301901
CDS Mutation	c.158G>A
AA Mutation	p.Arg53His(p.R53H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66643587:66643587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550G>A
AA Mutation	p.Ala184Thr(p.A184T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66643950:66643950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767778848
CDS Mutation	c.913G>A
AA Mutation	p.Gly305Arg(p.G305R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66639956:66639956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.245T>C
AA Mutation	p.Val82Ala(p.V82A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66640070:66640070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359G>A
AA Mutation	p.Arg120Gln(p.R120Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66644083:66644083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046G>A
AA Mutation	p.Arg349Gln(p.R349Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310092
Start	66643793:66643793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310092
Start	66643901:66643901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746731288
CDS Mutation	c.864T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RBM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66643456:66643456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419G>A
AA Mutation	p.Arg140Gln(p.R140Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66639801:66639801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90A>C
AA Mutation	p.Glu30Asp(p.E30D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310092
Start	66640038:66640038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000310092
Start	66639994:66639994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283C>T
AA Mutation	p.Arg95Ter(p.R95*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript