Colon Cancer: Gene >> NELFCD

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000602795
Start	58989639:58989639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710C>T
AA Mutation	p.Ala237Val(p.A237V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58989883:58989883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.737C>T
AA Mutation	p.Thr246Met(p.T246M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602795
Start	58991991:58991991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602795
Start	58987730:58987730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.363G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602795
Start	58990982:58990982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602795
Start	58991413:58991413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369337569
CDS Mutation	c.1110G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NELFCD

No Mutation Annotation!