Variant #0000535491 (NC_000008.10:g.95411702C>A, NM_012415.3:c.1318G>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.95411702C>A
DNA change (hg38) g.94399474C>A
Published as RAD54B(NM_001205263.1):c.766G>T (p.A256S)
ISCN -
DB-ID FSBP_000003
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FSBP NM_001256141.1 -?/. - c.*32657G>T r.(=) p.(=)
RAD54B NM_012415.3 -?/. - c.1318G>T r.(?) p.(Ala440Ser)


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