Colon Cancer: Gene >> RBFOX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7607326:7607326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664G>A
AA Mutation	p.Glu222Lys(p.E222K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7518325:7518325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206C>T
AA Mutation	p.Ala69Val(p.A69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7518264:7518264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755458164
CDS Mutation	c.145G>A
AA Mutation	p.Ala49Thr(p.A49T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7676805:7676805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962C>T
AA Mutation	p.Pro321Leu(p.P321L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7676798:7676798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199644500
CDS Mutation	c.955G>A
AA Mutation	p.Ala319Thr(p.A319T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7587290:7587290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.458G>A
AA Mutation	p.Arg153Gln(p.R153Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7518253:7518253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134A>G
AA Mutation	p.His45Arg(p.H45R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7710737:7710737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186C>T
AA Mutation	p.Pro396Ser(p.P396S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7709064:7709064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763620262
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335Gln(p.R335Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7518370:7518370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.251C>G
AA Mutation	p.Thr84Ser(p.T84S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7630653:7630653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>A
AA Mutation	p.Ala243Thr(p.A243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000547338
Start	7653843:7653843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755253534
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000547338
Start	7518236:7518236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771957716
CDS Mutation	c.117G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000547338
Start	7518266:7518266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752770034
CDS Mutation	c.147G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000547338
Start	7709106:7709106(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1050delC
AA Mutation	p.Thr351ProfsTer7(p.T351Pfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RBFOX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7676792:7676792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.949C>T
AA Mutation	p.Arg317Cys(p.R317C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7710729:7710729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178G>A
AA Mutation	p.Arg393His(p.R393H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000547338
Start	7518372:7518372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253G>A
AA Mutation	p.Val85Ile(p.V85I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript