Variant #0001026869 (NC_000017.10:g.33446607C>G, NM_002878.3:c.26G>C (RAD51D))

Chromosome 17
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.33446607C>G
DNA change (hg38) -
Published as RAD51D(NM_001142571.1):c.26G>C (p.(Cys9Ser))
ISCN -
DB-ID FNDC8_000014 See all 4 reported entries
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) 0.00036 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 2025-02-07 18:57:27 +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     
RAD51D NM_002878.3 ?/. - c.26G>C r.(?) p.(Cys9Ser)
FNDC8 NM_017559.2 ?/. - c.-2106C>G r.(?) p.(=)


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