Variant #0000866587 (NC_000020.10:g.62305313G>A, NM_016434.3:c.786G>A (RTEL1))

Chromosome 20
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.62305313G>A
DNA change (hg38) -
Published as RTEL1(NM_016434.3):c.786G>A (p.(=))
ISCN -
DB-ID ARFRP1_000091
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) 0.012 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARFRP1 NM_001134758.2 -/. - c.*26637C>T r.(=) p.(=)
TNFRSF6B NM_003823.3 -/. - c.-22808G>A r.(?) p.(=)
RTEL1 NM_016434.3 -/. - c.786G>A r.(?) p.(Ser262=)
RTEL1-TNFRSF6B NR_037882.1 -/. - n.1613G>A r.(?) -


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