Variant #0000931207 (NC_000020.10:g.62309621T>C, NM_016434.3:c.959T>C (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.62309621T>C
DNA change (hg38) -
Published as RTEL1(NM_001283009.1):c.959T>C (p.M320T, p.(Met320Thr)), RTEL1(NM_001283010.1):c.290T>C (p.M97T), RTEL1(NM_032957.5):c.1031T>C (p.M344T)
ISCN -
DB-ID ARFRP1_000004 See all 4 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) 0.00115 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 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARFRP1 NM_001134758.2 -?/. - c.*22329A>G r.(=) p.(=)
TNFRSF6B NM_003823.3 -?/. - c.-18500T>C r.(?) p.(=)
RTEL1 NM_016434.3 -?/. - c.959T>C r.(?) p.(Met320Thr)
RTEL1-TNFRSF6B NR_037882.1 -?/. - n.1786T>C r.(?) -


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