Variant #0000894055 (NC_000017.10:g.56772284A>G, NC_000017.10(NM_058216.1):c.146-8A>G (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.56772284A>G
DNA change (hg38) -
Published as RAD51C(NM_002876.2):c.146-8A>G (p.(=)), RAD51C(NM_058216.1):c.146-8A>G, RAD51C(NM_058216.3):c.146-8A>G
ISCN -
DB-ID RAD51C_000028 See all 7 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) 0.00122 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.-2986T>C r.(?) p.(=) -
RAD51C NM_058216.1 -/. - c.146-8A>G r.(=) p.(=) -


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