Variant #0000805789 (NC_000012.11:g.50042816_50042817dup, NM_175736.4:c.2510_2511dup (FMNL3))

Chromosome 12
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.50042816_50042817dup
DNA change (hg38) -
Published as FMNL3(NM_175736.4):c.2511_2512insCA (p.(Ala838Glnfs*12))
ISCN -
DB-ID FMNL3_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2021-09-17 14:40:49 +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     
PRPF40B NM_001031698.2 +?/. - c.*4841_*4842dup r.(=) p.(=)
FMNL3 NM_175736.4 +?/. - c.2510_2511dup r.(?) p.(Ala838Glnfs*12)


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