Variant #0000301338 (NC_000008.10:g.117868553_117868554del, NC_000008.10(NM_006265.2):c.815-6_815-5del (RAD21))

Chromosome 8
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.117868553_117868554del
DNA change (hg38) g.116856314_116856315del
Published as RAD21(NM_006265.2):c.815-6_815-5del (p.?), RAD21(NM_006265.2):c.815-6_815-5delTT
ISCN -
DB-ID RAD21_000006 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD21 NM_006265.2 -/. - c.815-6_815-5del r.spl? p.?


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