Variant #0000894346 (NC_000017.10:g.78360617_78360619del, NM_001256071.1:c.14848_14850del (RNF213))

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.78360617_78360619del
DNA change (hg38) -
Published as RNF213(NM_001256071.2):c.14848_14850delGAG (p.E4950del)
ISCN -
DB-ID ENDOV_000013
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF213 NM_001256071.1 ?/. - c.14848_14850del r.(?) p.(Glu4950del)
ENDOV NM_173627.3 ?/. - c.-28378_-28376del r.(?) p.(=)


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