Colon Cancer: Gene >> FAM3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357985
Start	41323045:41323045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142G>T
AA Mutation	p.Gly48Trp(p.G48W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357985
Start	41322942:41322942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186901119
CDS Mutation	c.39C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357985
Start	41347086:41347086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144944684
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357985
Start	41347089:41347089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573794470
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357985
Start	41348720:41348720(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.617delA
AA Mutation	p.Lys206ArgfsTer21(p.K206Rfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FAM3B

No Mutation Annotation!