Variant #0001053056 (NC_000008.10:g.95416309T>A, NM_012415.3:c.940A>T (RAD54B))

Chromosome 8
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.95416309T>A
DNA change (hg38) -
Published as RAD54B(NM_012415.3):c.940A>T (p.(Met314Leu))
ISCN -
DB-ID FSBP_000005
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) 0.00367 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FSBP NM_001256141.1 -?/. - c.*28050A>T r.(=) p.(=)
RAD54B NM_012415.3 -?/. - c.940A>T r.(?) p.(Met314Leu)


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