Variant #0000692542 (NC_000017.10:g.8192382G>T, NM_016492.4:c.186G>T (RANGRF))

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.8192382G>T
DNA change (hg38) -
Published as RANGRF(NM_001177802.2):c.186G>T (p.A62=)
ISCN -
DB-ID RANGRF_000014
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-09-15 15:50:26 +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     
RANGRF NM_016492.4 -/. - c.186G>T r.(?) p.(Ala62=)
SLC25A35 NM_201520.1 -/. - c.*552C>A r.(=) p.(=)


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