Variant #0000524148 (NC_000005.9:g.131911535A>C, NM_005732.3:c.280A>C (RAD50))

Chromosome 5
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.131911535A>C
DNA change (hg38) g.132575843A>C
Published as RAD50(NM_005732.3):c.280A>C (p.I94L), RAD50(NM_005732.4):c.280A>C (p.I94L)
ISCN -
DB-ID RAD50_000019 See all 2 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) 0.00347 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-06 12:43:26 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD50 NM_005732.3 -?/. - c.280A>C r.(?) p.(Ile94Leu)


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