Variant #0000787535 (NC_000023.10:g.?, FLNA(NM_001110556.1):c.?)

Individual ID 00374542
Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.?
DNA change (hg38) -
Published as c.1807G>A p.Gly603Arg)
ISCN -
DB-ID USP9X_000005 See all 209 reported entries
Variant remarks -
Reference 0
ClinVar ID -
dbSNP ID rs200116438
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner LOVD
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLNA NM_001110556.1 ?/. 12 c.? r.? p.?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000375736 DNA SEQ-NG - TruSight One panel CYB5R3 3 Johan den Dunnen