Variant #0000927054 (NC_000020.10:g.62324292C>T, NM_016434.3:c.2787C>T (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.62324292C>T
DNA change (hg38) -
Published as RTEL1(NM_001283009.1):c.2787C>T (p.A929=), RTEL1(NM_001283010.1):c.2118C>T (p.A706=)
ISCN -
DB-ID RTEL1-TNFRSF6B_000022 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) 0.0006 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.*7658G>A r.(=) p.(=)
TNFRSF6B NM_003823.3 -?/. - c.-3829C>T r.(?) p.(=)
RTEL1 NM_016434.3 -?/. - c.2787C>T r.(?) p.(Ala929=)
RTEL1-TNFRSF6B NR_037882.1 -?/. - n.3614C>T r.(?) -


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