Variant #0000001366 (NC_000017.10:g.42428803delC, GRN(NM_002087.2):c.908delC)

Individual ID 00001366
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.42428803delC
Reference Lladó A1, Sánchez-Valle R, Re?é R, Ezquerra M, Rey MJ, Tolosa E, Ferrer I, Molinuevo JL.(2007)
DB-ID GRN_000030
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
GRN NM_002087.2 ./. 9 c.908delC r.(?) p.(Trp304Glyfs*57) VariO:0141 DNA deletion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001366 ? ? GRN 1 Y Yang