Variant #0001067381 (NC_000020.10:g.62316953_62317030del, NC_000020.10(NM_016434.3):c.1266+3_1266+80del (RTEL1))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.62316953_62317030del
DNA change (hg38) -
Published as -
ISCN -
DB-ID ARFRP1_000150
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +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     
ARFRP1 NM_001134758.2 +?/. - c.*14952_*15029del r.(=) p.(=)
TNFRSF6B NM_003823.3 +?/. - c.-11168_-11091del r.(?) p.(=)
RTEL1 NM_016434.3 +?/. - c.1266+3_1266+80del r.spl? p.?
RTEL1-TNFRSF6B NR_037882.1 +?/. - n.2093+3_2093+80del r.(?) -


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