Variant #0000563829 (NC_000017.10:g.8192188G>A, NC_000017.10(NM_016492.4):c.77+5G>A (RANGRF))

Chromosome 17
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.8192188G>A
DNA change (hg38) g.8288870G>A
Published as RANGRF(NM_001177802.2):c.77+5G>A, SLC25A35(NM_201520.3):c.*746C>T
ISCN -
DB-ID RANGRF_000010
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) 0.00026 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-13 08:34:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RANGRF NM_016492.4 -?/. - c.77+5G>A r.spl? p.?
SLC25A35 NM_201520.1 -?/. - c.*746C>T r.(=) p.(=)


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