Colon Cancer: Gene >> LPAR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370611
Start	84865846:84865846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275C>T
AA Mutation	p.Pro92Leu(p.P92L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370611
Start	84865484:84865484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637G>A
AA Mutation	p.Val213Ile(p.V213I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370611
Start	84865490:84865490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149590072
CDS Mutation	c.631G>A
AA Mutation	p.Val211Met(p.V211M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370611
Start	84814012:84814012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896A>G
AA Mutation	p.Asp299Gly(p.D299G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370611
Start	84865538:84865538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.583A>G
AA Mutation	p.Asn195Asp(p.N195D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370611
Start	84865638:84865638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752564044
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370611
Start	84865464:84865464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.657C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LPAR3

No Mutation Annotation!