Variant #0001006583 (NC_000023.10:g.153607863C>G, NM_001110556.1:c.-5106G>C (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.153607863C>G
DNA change (hg38) -
Published as EMD(NM_000117.3):c.19C>G (p.L7V)
ISCN -
DB-ID FLNA_000556
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EMD NM_000117.2 ?/. - c.19C>G r.(?) p.(Leu7Val)
FLNA NM_001110556.1 ?/. - c.-5106G>C r.(?) p.(=)


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