Variant #0000332209 (NC_000008.10:g.95406068A>G, NM_012415.3:c.1421T>C (RAD54B))

Chromosome 8
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.95406068A>G
DNA change (hg38) g.94393840A>G
Published as RAD54B(NM_001205263.1):c.869T>C (p.(Ile290Thr))
ISCN -
DB-ID RAD54B_000001
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 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 2018-01-15 20:58:59 +01:00 (CET)
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.*38291T>C r.(=) p.(=)
RAD54B NM_012415.3 ?/. - c.1421T>C r.(?) p.(Ile474Thr)


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