Variant #0000866593 (NC_000020.10:g.62326498G>A, NM_016434.3:c.3423G>A (RTEL1))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.62326498G>A
DNA change (hg38) -
Published as RTEL1(NM_001283009.1):c.3423G>A (p.P1141=, p.(Pro1141=)), RTEL1(NM_001283010.1):c.2754G>A (p.P918=)
ISCN -
DB-ID RTEL1-TNFRSF6B_000028 See all 3 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) 0.00156 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 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     
ZGPAT NM_001083113.1 -?/. - c.-12442G>A r.(?) p.(=)
ARFRP1 NM_001134758.2 -?/. - c.*5452C>T r.(=) p.(=)
TNFRSF6B NM_003823.3 -?/. - c.-1623G>A r.(?) p.(=)
RTEL1 NM_016434.3 -?/. - c.3423G>A r.(?) p.(Pro1141=)
RTEL1-TNFRSF6B NR_037882.1 -?/. - n.4250G>A r.(?) -


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