Variant #0001031409 (NC_000001.10:g.161183716G>A, NM_004106.1:c.-1396G>A (FCER1G))

Chromosome 1
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.161183716G>A
DNA change (hg38) -
Published as NDUFS2(NM_001377299.1):c.1354+5G>A
ISCN -
DB-ID ADAMTS4_000013
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) 0.00031 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
FCER1G NM_004106.1 ?/. - c.-1396G>A r.(?) p.(=)
NDUFS2 NM_004550.4 ?/. - c.1354+5G>A r.spl? p.?
ADAMTS4 NM_005099.4 ?/. - c.-15299C>T r.(?) p.(=)


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