Variant #0001027462 (NC_000023.10:g.153599552_153599554dup, NM_001110556.1:c.62_64dup (FLNA))

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.153599552_153599554dup
DNA change (hg38) -
Published as FLNA(NM_001110556.1):c.64_65insTCG (p.(Val21dup)), FLNA(NM_001110556.2):c.58_60dupTCG (p.V21dup), FLNA(NM_001110556.2):c.62_64dupTCG (p.V21dup)
ISCN -
DB-ID FLNA_000281 See all 5 reported entries
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLNA NM_001110556.1 ?/. - c.62_64dup r.(?) p.(Val21dup)


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