Variant #0000306786 (NC_000018.9:g.20573013_20573018del, NM_002894.2:c.1223_1228del (RBBP8))

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.20573013_20573018del
DNA change (hg38) g.22993050_22993055del
Published as RBBP8(NM_002894.2):c.1223_1228delTAAATA (p.I408_N409del)
ISCN -
DB-ID RBBP8_000009
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBBP8 NM_002894.2 ?/. - c.1223_1228del r.(?) p.(Ile408_Asn409del)


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