Variant #0000854836 (NC_000017.10:g.33444067del, NC_000017.10(NM_002878.3):c.263+1455del (RAD51D))

Chromosome 17
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.33444067del
DNA change (hg38) -
Published as RAD51D(NM_002878.3):c.263+1455delA
ISCN -
DB-ID FNDC8_000022
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_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2022-05-09 15:47:41 +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     
RAD51D NM_002878.3 -?/. - c.263+1455del r.(=) p.(=)
FNDC8 NM_017559.2 -?/. - c.-4646del r.(?) p.(=)


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