Colon Cancer: Gene >> GPR39

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132417169:132417169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127A>G
AA Mutation	p.Met43Val(p.M43V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132417390:132417390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348G>T
AA Mutation	p.Glu116Asp(p.E116D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132645220:132645220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976C>A
AA Mutation	p.Leu326Ile(p.L326I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132417641:132417641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599A>C
AA Mutation	p.Glu200Ala(p.E200A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329321
Start	132645288:132645288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758833762
CDS Mutation	c.1044G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329321
Start	132645336:132645336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1092G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329321
Start	132417531:132417531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756802505
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329321
Start	132417834:132417834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329321
Start	132417567:132417567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329321
Start	132645378:132645378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329321
Start	132645396:132645396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142925280
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPR39

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132417727:132417727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685G>A
AA Mutation	p.Val229Met(p.V229M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329321
Start	132645543:132645543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1299C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329321
Start	132417154:132417154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.112C>T
Mutation Classification	Silent
Feature Type	Transcript