Colon Cancer: Gene >> FAIM2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000320634
Start	49901130:49901130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211A>T
AA Mutation	p.Ser71Cys(p.S71C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320634
Start	49890688:49890688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773139598
CDS Mutation	c.520G>A
AA Mutation	p.Val174Ile(p.V174I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320634
Start	49901168:49901168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145638550
CDS Mutation	c.173C>T
AA Mutation	p.Ala58Val(p.A58V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320634
Start	49901185:49901185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156C>A
AA Mutation	p.Phe52Leu(p.F52L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320634
Start	49889526:49889526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765147386
CDS Mutation	c.606G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320634
Start	49889511:49889511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375275250
CDS Mutation	c.621C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320634
Start	49889155:49889155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000320634
Start	49898004:49898004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Ter(p.R100*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FAIM2

No Mutation Annotation!