Colon Cancer: Gene >> OSM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215781
Start	30264119:30264119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529069377
CDS Mutation	c.523C>T
AA Mutation	p.Pro175Ser(p.P175S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215781
Start	30264310:30264310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332C>A
AA Mutation	p.Ala111Asp(p.A111D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000215781
Start	30263941:30263941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701G>T
AA Mutation	p.Arg234Met(p.R234M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000215781
Start	30264308:30264308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535625269
CDS Mutation	c.334G>A
AA Mutation	p.Asp112Asn(p.D112N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215781
Start	30266790:30266790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000215781
Start	30264002:30264002(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776089535
CDS Mutation	c.640delG
AA Mutation	p.Glu214ArgfsTer15(p.E214Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000215781
Start	30265145:30265145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> OSM

No Mutation Annotation!