Variant #0000951488 (NC_000020.10:g.62324513C>T, NM_016434.3:c.2869C>T (RTEL1))

Chromosome 20
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.62324513C>T
DNA change (hg38) -
Published as RTEL1(NM_032957.5):c.2941C>T (p.R981W)
ISCN -
DB-ID ARFRP1_000031 See all 2 reported entries
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +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.*7437G>A r.(=) p.(=)
TNFRSF6B NM_003823.3 +/. - c.-3608C>T r.(?) p.(=)
RTEL1 NM_016434.3 +/. - c.2869C>T r.(?) p.(Arg957Trp)
RTEL1-TNFRSF6B NR_037882.1 +/. - n.3696C>T r.(?) -


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