Variant #0000564104 (NC_000018.9:g.20577578_20577581del, NC_000018.9(NM_002894.2):c.2029-5_2029-2del (RBBP8))

Chromosome 18
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.20577578_20577581del
DNA change (hg38) g.22997615_22997618del
Published as RBBP8(NM_002894.2):c.2029-11_2029-8del (p.(=))
ISCN -
DB-ID RBBP8_000021
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-14 17:02:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBBP8 NM_002894.2 -?/. - c.2029-5_2029-2del r.spl? p.?


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