Colon Cancer: Gene >> LONP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360614
Start	5693733:5693733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756015513
CDS Mutation	c.2357G>A
AA Mutation	p.Arg786Gln(p.R786Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360614
Start	5707821:5707821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.938C>T
AA Mutation	p.Ser313Leu(p.S313L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360614
Start	5696142:5696142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371606894
CDS Mutation	c.1925C>T
AA Mutation	p.Thr642Met(p.T642M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360614
Start	5707714:5707714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199733142
CDS Mutation	c.1045G>A
AA Mutation	p.Val349Ile(p.V349I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360614
Start	5719966:5719966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.167G>T
AA Mutation	p.Gly56Val(p.G56V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360614
Start	5692156:5692156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2756A>T
AA Mutation	p.Asp919Val(p.D919V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360614
Start	5696337:5696337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746766577
CDS Mutation	c.1808C>T
AA Mutation	p.Pro603Leu(p.P603L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360614
Start	5692082:5692082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138631909
CDS Mutation	c.2830G>A
AA Mutation	p.Asp944Asn(p.D944N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360614
Start	5694879:5694879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549574673
CDS Mutation	c.2036G>A
AA Mutation	p.Arg679His(p.R679H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000360614
Start	5696755:5696755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1688G>A
AA Mutation	p.Arg563Gln(p.R563Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360614
Start	5719797:5719797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360614
Start	5714206:5714206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146460691
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360614
Start	5694887:5694887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2028C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360614
Start	5707131:5707131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360614
Start	5696258:5696258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1887C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360614
Start	5694833:5694833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770545248
CDS Mutation	c.2082C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LONP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360614
Start	5700796:5700796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368654972
CDS Mutation	c.1499G>A
AA Mutation	p.Arg500His(p.R500H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360614
Start	5693594:5693594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2496T>C
Mutation Classification	Silent
Feature Type	Transcript