Variant #0000865506 (NC_000017.10:g.74468763C>T, NC_000017.10(NM_024599.5):c.2151+5G>A (RHBDF2))

Chromosome 17
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.74468763C>T
DNA change (hg38) -
Published as RHBDF2(NM_024599.5):c.2151+5G>A
ISCN -
DB-ID AANAT_000005
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AANAT NM_001088.2 ?/. - c.*2711C>T r.(=) p.(=)
RHBDF2 NM_024599.5 ?/. - c.2151+5G>A r.spl? p.?


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