Colon Cancer: Gene >> NPRL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000611875
Start	98268:98268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801G>T
AA Mutation	p.Glu267Asp(p.E267D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000611875
Start	138155:138155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113A>T
AA Mutation	p.Gln38Leu(p.Q38L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000611875
Start	86809:86809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769327693
CDS Mutation	c.1606C>T
AA Mutation	p.Arg536Trp(p.R536W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000611875
Start	88884:88884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358G>A
AA Mutation	p.Ser453Asn(p.S453N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000611875
Start	100499:100499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.640T>C
AA Mutation	p.Ser214Pro(p.S214P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000611875
Start	89734:89734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368198378
CDS Mutation	c.1330G>A
AA Mutation	p.Ala444Thr(p.A444T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000611875
Start	100498:100498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556232826
CDS Mutation	c.641C>T
AA Mutation	p.Ser214Leu(p.S214L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611875
Start	93251:93251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611875
Start	112722:112722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367592989
CDS Mutation	c.447C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611875
Start	112761:112761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757635247
CDS Mutation	c.408G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NPRL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000611875
Start	117327:117327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367C>A
AA Mutation	p.Leu123Ile(p.L123I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript