Colon Cancer: Gene >> NAGLU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225927
Start	42543553:42543553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773054539
CDS Mutation	c.1547C>T
AA Mutation	p.Pro516Leu(p.P516L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225927
Start	42543241:42543241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1235G>A
AA Mutation	p.Gly412Glu(p.G412E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225927
Start	42544063:42544063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760257524
CDS Mutation	c.2057T>C
AA Mutation	p.Val686Ala(p.V686A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225927
Start	42541185:42541185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749140168
CDS Mutation	c.1000G>A
AA Mutation	p.Val334Ile(p.V334I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000225927
Start	42537460:42537460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446G>A
AA Mutation	p.Arg149His(p.R149H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000225927
Start	42543135:42543135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1129C>A
AA Mutation	p.Arg377Ser(p.R377S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225927
Start	42544214:42544214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759014662
CDS Mutation	c.2208C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225927
Start	42536620:42536620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559674042
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225927
Start	42544049:42544049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115401566
CDS Mutation	c.2043G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225927
Start	42543065:42543065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1059C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NAGLU

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225927
Start	42544049:42544049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115401566
CDS Mutation	c.2043G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000225927
Start	42541077:42541077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.892G>T
AA Mutation	p.Glu298Ter(p.E298*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript