Colon Cancer: Gene >> FAM3D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358781
Start	58643686:58643686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298G>T
AA Mutation	p.Gly100Cys(p.G100C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358781
Start	58653692:58653692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140921588
CDS Mutation	c.103C>T
AA Mutation	p.Arg35Cys(p.R35C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358781
Start	58653741:58653741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358781
Start	58636354:58636354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358781
Start	58645529:58645529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358781
Start	58637183:58637183(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.416delG
AA Mutation	p.Gly139ValfsTer16(p.G139Vfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FAM3D

No Mutation Annotation!