Variant #0000299315 (NC_000017.10:g.74470523G>A, NM_024599.5:c.1483C>T (RHBDF2))

Chromosome 17
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.74470523G>A
DNA change (hg38) g.76474441G>A
Published as RHBDF2(NM_024599.5):c.1483C>T (p.R495W)
ISCN -
DB-ID RHBDF2_000009 See all 3 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) 0.0032 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AANAT NM_001088.2 -/. - c.*4471G>A r.(=) p.(=)
RHBDF2 NM_024599.5 -/. - c.1483C>T r.(?) p.(Arg495Trp)


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