Colon Cancer: Gene >> RFX1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000254325
Start	13968679:13968679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1618C>T
AA Mutation	p.Leu540Phe(p.L540F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254325
Start	13965658:13965658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2081T>C
AA Mutation	p.Ile694Thr(p.I694T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254325
Start	13980605:13980605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374974524
CDS Mutation	c.706G>A
AA Mutation	p.Gly236Ser(p.G236S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254325
Start	13980682:13980682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629C>T
AA Mutation	p.Pro210Leu(p.P210L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254325
Start	13983223:13983223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254325
Start	13972839:13972839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765259605
CDS Mutation	c.1218C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254325
Start	13965645:13965645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139336544
CDS Mutation	c.2094C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254325
Start	13982196:13982196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs80165125
CDS Mutation	c.546C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254325
Start	13966500:13966522(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1860_1882delCGACGTCATGGTGAACCTGCAGT
AA Mutation	p.Asp621HisfsTer20(p.D621Hfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000254325
Start	13963704:13963704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2404C>T
AA Mutation	p.Gln802Ter(p.Q802*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RFX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254325
Start	13965454:13965454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2206G>T
AA Mutation	p.Val736Leu(p.V736L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript