Variant #0000895438 (NC_000020.10:g.62324579C>T, NM_016434.3:c.2935C>T (RTEL1))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.62324579C>T
DNA change (hg38) -
Published as RTEL1(NM_001283009.1):c.2935C>T (p.(Arg979Trp)), RTEL1(NM_032957.5):c.3007C>T (p.R1003W)
ISCN -
DB-ID ARFRP1_000105 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) 0.0001 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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.*7371G>A r.(=) p.(=)
TNFRSF6B NM_003823.3 ?/. - c.-3542C>T r.(?) p.(=)
RTEL1 NM_016434.3 ?/. - c.2935C>T r.(?) p.(Arg979Trp)
RTEL1-TNFRSF6B NR_037882.1 ?/. - n.3762C>T r.(?) -


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