Colon Cancer: Gene >> CRISP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000433368
Start	49728735:49728735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802T>A
AA Mutation	p.Tyr268Asn(p.Y268N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000433368
Start	49733846:49733846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349C>A
AA Mutation	p.Leu117Ile(p.L117I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000433368
Start	49731231:49731231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759469703
CDS Mutation	c.611T>C
AA Mutation	p.Leu204Pro(p.L204P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000433368
Start	49731225:49731225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617T>C
AA Mutation	p.Val206Ala(p.V206A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000433368
Start	49736427:49736427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222A>T
AA Mutation	p.Arg74Ser(p.R74S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433368
Start	49731170:49731170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.672A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433368
Start	49733805:49733805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433368
Start	49736466:49736466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CRISP3

No Mutation Annotation!