Variant #0000950956 (NC_000017.10:g.56770094G>A, NM_058216.1:c.90G>A (RAD51C))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56770094G>A
DNA change (hg38) -
Published as RAD51C(NM_002876.2):c.90G>A (p.(Ala30=)), RAD51C(NM_058216.1):c.90G>A (p.A30=)
ISCN -
DB-ID TEX14_000010 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) 0.00264 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +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     

Haplotype     
TEX14 NM_001201457.1 -/. - c.-796C>T r.(?) p.(=) -
RAD51C NM_058216.1 -/. - c.90G>A r.(?) p.(Ala30=) -


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