Variant #0000682156 (NC_000023.10:g.147003504G>A, FMR1(NM_002024.5):c.104+1G>A)

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.147003504G>A
DNA change (hg38) -
Published as FMR1(NM_002024.5):c.104+1G>A (p.?)
ISCN -
DB-ID FMR1_000099
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMR1 NM_002024.5 +?/. - c.104+1G>A - r.spl? p.?
FMR1-AS1 NR_024499.1 +?/. - n.173C>T - r.(?) -