Colon Cancer: Gene >> LONRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398246
Start	12729190:12729190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1831A>G
AA Mutation	p.Ser611Gly(p.S611G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398246
Start	12725825:12725825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2065T>A
AA Mutation	p.Ser689Thr(p.S689T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398246
Start	12723181:12723181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759684068
CDS Mutation	c.2237C>T
AA Mutation	p.Ser746Leu(p.S746L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398246
Start	12729026:12729026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1885G>A
AA Mutation	p.Val629Met(p.V629M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398246
Start	12736960:12736960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1294C>A
AA Mutation	p.Leu432Ile(p.L432I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398246
Start	12729181:12729181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1840C>G
AA Mutation	p.Gln614Glu(p.Q614E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398246
Start	12735369:12735369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483G>A
AA Mutation	p.Gly495Arg(p.G495R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398246
Start	12729323:12729323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1698G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398246
Start	12728976:12728976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1935G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398246
Start	12725781:12725781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2109A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398246
Start	12729009:12729009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368962131
CDS Mutation	c.1902C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398246
Start	12740953:12740953(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.884delT
AA Mutation	p.Leu295Ter(p.L295*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000398246
Start	12725783:12725783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780246552
CDS Mutation	c.2107C>T
AA Mutation	p.Arg703Ter(p.R703*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000398246
Start	12725797:12725797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2093T>A
AA Mutation	p.Leu698Ter(p.L698*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398246
Start	12731766:12731767(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1657dupA
AA Mutation	p.Ile553AsnfsTer3(p.I553Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LONRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398246
Start	12729001:12729001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1910C>T
AA Mutation	p.Ser637Phe(p.S637F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398246
Start	12736721:12736721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769049327
CDS Mutation	c.1431C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000398246
Start	12729235:12729235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1786C>T
AA Mutation	p.Arg596Ter(p.R596*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript