Colon Cancer: Gene >> LRPAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000500728
Start	3520155:3520155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.388G>T
AA Mutation	p.Ala130Ser(p.A130S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000500728
Start	3516151:3516151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755497927
CDS Mutation	c.799G>A
AA Mutation	p.Ala267Thr(p.A267T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000500728
Start	3520154:3520154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.389C>T
AA Mutation	p.Ala130Val(p.A130V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000500728
Start	3520088:3520088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.455A>T
AA Mutation	p.Glu152Val(p.E152V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000500728
Start	3514911:3514911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776519916
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000500728
Start	3516140:3516140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572287773
CDS Mutation	c.810G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000500728
Start	3532323:3532323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LRPAP1

No Mutation Annotation!