Variant #0000654059 (NC_000001.10:g.46727058G>A, NC_000001.10(NM_003579.3):c.891+1G>A (RAD54L))

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.46727058G>A
DNA change (hg38) g.46261386G>A
Published as -
ISCN -
DB-ID RAD54L_000002
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-04 14:04:24 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD54L NM_003579.3 ?/. - c.891+1G>A r.spl? p.?
LRRC41 NM_006369.4 ?/. - c.*17479C>T r.(=) p.(=)


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