Colon Cancer: Gene >> RMDN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000406452
Start	86474921:86474921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756781000
CDS Mutation	c.793C>A
AA Mutation	p.Leu265Ile(p.L265I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000406452
Start	86474354:86474354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899A>G
AA Mutation	p.Gln300Arg(p.Q300R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000406452
Start	86486602:86486602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200295883
CDS Mutation	c.377G>A
AA Mutation	p.Arg126His(p.R126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406452
Start	86480291:86480291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.627C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000406452
Start	86488634:86488634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253G>T
AA Mutation	p.Glu85Ter(p.E85*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000406452
Start	86486508:86486509(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.470dupA
AA Mutation	p.Asn157LysfsTer2(p.N157Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RMDN1

No Mutation Annotation!