Variant #0001005576 (NC_000020.10:g.62292738C>T, NM_016434.3:c.190C>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.62292738C>T
DNA change (hg38) -
Published as RTEL1(NM_001283009.1):c.190C>T (p.(Arg64*))
ISCN -
DB-ID RTEL1_000001 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
ARFRP1 NM_001134758.2 ?/. - c.*39212G>A r.(=) p.(=)
TNFRSF6B NM_003823.3 ?/. - c.-35383C>T r.(?) p.(=)
RTEL1 NM_016434.3 ?/. - c.190C>T r.(?) p.(Arg64*)
RTEL1-TNFRSF6B NR_037882.1 ?/. - n.1017C>T r.(?) -


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