Variant #0001032108 (NC_000001.10:g.46739327G>A, NM_003579.3:c.1518G>A (RAD54L))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46739327G>A
DNA change (hg38) -
Published as RAD54L(NM_003579.4):c.1518G>A (p.(Ala506=))
ISCN -
DB-ID RAD54L_000006
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) 0.00082 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     
RAD54L NM_003579.3 -?/. - c.1518G>A r.(?) p.(=)
LRRC41 NM_006369.4 -?/. - c.*5210C>T r.(=) p.(=)


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