Variant #0000950837 (NC_000017.10:g.33446133G>C, NM_002878.3:c.141C>G (RAD51D))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.33446133G>C
DNA change (hg38) -
Published as RAD51D(NM_002878.3):c.141C>G (p.Y47*), RAD51D(NM_002878.4):c.141C>G (p.Y47*)
ISCN -
DB-ID FNDC8_000029 See all 3 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) 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 2023-11-27 17:35:39 +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.141C>G r.(?) p.(Tyr47*)
FNDC8 NM_017559.2 +/. - c.-2580G>C r.(?) p.(=)


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