Colon Cancer: Gene >> ENPP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328313
Start	79733519:79733519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574138520
CDS Mutation	c.265G>A
AA Mutation	p.Glu89Lys(p.E89K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328313
Start	79735334:79735334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201532960
CDS Mutation	c.691G>A
AA Mutation	p.Ala231Thr(p.A231T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328313
Start	79735293:79735293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372350760
CDS Mutation	c.650G>A
AA Mutation	p.Arg217Gln(p.R217Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328313
Start	79735337:79735337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782703540
CDS Mutation	c.694C>T
AA Mutation	p.Arg232Cys(p.R232C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328313
Start	79735493:79735493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850G>T
AA Mutation	p.Gly284Trp(p.G284W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328313
Start	79735246:79735246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201933801
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328313
Start	79731319:79731319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782026581
CDS Mutation	c.180C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ENPP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328313
Start	79731239:79731239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100C>T
AA Mutation	p.Leu34Phe(p.L34F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328313
Start	79731295:79731295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript