Variant #0000619299 (NC_000023.10:g.153599528_153599529insTA, FLNA(NM_001110556.1):c.85_86insTA)

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.153599528_153599529insTA
DNA change (hg38) g.154371160_154371161insTA
Published as FLNA(NM_001110556.1):c.85_86insTA (p.(Pro29LeufsTer30))
ISCN -
DB-ID FLNA_000430
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLNA NM_001110556.1 ?/. - c.85_86insTA r.(?) p.(Pro29LeufsTer30)