Colon Cancer: Gene >> RFX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290524
Start	151342635:151342635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745673103
CDS Mutation	c.1402C>T
AA Mutation	p.Arg468Cys(p.R468C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290524
Start	151342641:151342641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1396C>T
AA Mutation	p.Arg466Trp(p.R466W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290524
Start	151344429:151344429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142678277
CDS Mutation	c.461G>A
AA Mutation	p.Arg154Gln(p.R154Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290524
Start	151342454:151342454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1583C>T
AA Mutation	p.Ala528Val(p.A528V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000290524
Start	151342357:151342357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1680G>T
AA Mutation	p.Leu560Phe(p.L560F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000290524
Start	151343156:151343156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777652681
CDS Mutation	c.881G>A
AA Mutation	p.Arg294Gln(p.R294Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000290524
Start	151346272:151346272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>C
AA Mutation	p.Ala17Pro(p.A17P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290524
Start	151342978:151342978(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1059delC
AA Mutation	p.Arg354GlyfsTer7(p.R354Gfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290524
Start	151346265:151346265(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.56delC
AA Mutation	p.Pro19GlnfsTer28(p.P19Qfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290524
Start	151342585:151342586(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1451_1452delTC
AA Mutation	p.Leu484GlnfsTer41(p.L484Qfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290524
Start	151343034:151343034(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1003delC
AA Mutation	p.Arg335GlyfsTer6(p.R335Gfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290524
Start	151343093:151343093(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.944delC
AA Mutation	p.Pro315GlnfsTer11(p.P315Qfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000290524
Start	151346218:151346218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103C>T
AA Mutation	p.Arg35Ter(p.R35*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000290524
Start	151342839:151342839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766158684
CDS Mutation	c.1198C>T
AA Mutation	p.Arg400Ter(p.R400*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000290524
Start	151343884:151343884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RFX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290524
Start	151344427:151344427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463G>A
AA Mutation	p.Gly155Ser(p.G155S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290524
Start	151342765:151342765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1272A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000290524
Start	151346481:151346481(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.-14+1delG
Mutation Classification	Splice_Site
Feature Type	Transcript