Variant #0000297538 (NC_000017.10:g.33445642C>T, NC_000017.10(NM_002878.3):c.145-4G>A (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.33445642C>T
DNA change (hg38) g.35118623C>T
Published as RAD51D(NM_001142571.2):c.144+488G>A, RAD51D(NM_002878.4):c.145-4G>A
ISCN -
DB-ID RAD51D_000010 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) 0.00012 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD51D NM_002878.3 -?/. - c.145-4G>A r.spl? p.?
FNDC8 NM_017559.2 -?/. - c.-3071C>T r.(?) p.(=)


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