Colon Cancer: Gene >> RAPGEF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47757902:47757902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183G>T
AA Mutation	p.Glu61Asp(p.E61D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47747617:47747617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1483G>A
AA Mutation	p.Asp495Asn(p.D495N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47737590:47737590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2749C>A
AA Mutation	p.Leu917Ile(p.L917I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47740666:47740666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2207G>A
AA Mutation	p.Arg736Lys(p.R736K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47747842:47747842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1343G>A
AA Mutation	p.Gly448Asp(p.G448D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47748852:47748852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121G>A
AA Mutation	p.Gly374Asp(p.G374D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47750414:47750414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779519570
CDS Mutation	c.683G>A
AA Mutation	p.Arg228His(p.R228H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47739164:47739164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2440T>C
AA Mutation	p.Phe814Leu(p.F814L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47751084:47751084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.635G>A
AA Mutation	p.Gly212Glu(p.G212E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47750354:47750354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.743A>G
AA Mutation	p.His248Arg(p.H248R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389212
Start	47751152:47751152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61733250
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389212
Start	47737597:47737597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2742C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389212
Start	47746872:47746872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1584T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389212
Start	47757986:47757986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389212
Start	47738035:47738035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747340295
CDS Mutation	c.2640G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389212
Start	47751146:47751146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RAPGEF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47751811:47751811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>T
AA Mutation	p.Leu98Phe(p.L98F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47743668:47743668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1687G>A
AA Mutation	p.Asp563Asn(p.D563N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389212
Start	47740380:47740380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2247G>T
AA Mutation	p.Lys749Asn(p.K749N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389212
Start	47740680:47740680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2193G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000389212
Start	47743605:47743605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750G>T
AA Mutation	p.Glu584Ter(p.E584*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript