Variant #0000001391 (NC_000017.10:g.42428507_42428510delCTCA, GRN(NM_002087.2):c.811_814delCTCA)

Individual ID 00001391
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.42428507_42428510delCTCA
Reference Benussi L1, Binetti G, Sina E, Gigola L, Bettecken T, Meitinger T, Ghidoni R.(2008)
DB-ID GRN_000065
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 ./. 8 c.811_814delCTCA r.(?) p.(Thr272Serfs*10) VariO:0141 DNA deletion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001391 ? ? GRN 1 Y Yang