Variant #0000895437 (NC_000020.10:g.62324559C>T, NM_016434.3:c.2915C>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.62324559C>T
DNA change (hg38) -
Published as RTEL1(NM_001283010.1):c.2246C>T (p.T749I)
ISCN -
DB-ID ARFRP1_000104
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) 0.00026 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 2022-11-01 13:41:49 +01:00 (CET)
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.*7391G>A r.(=) p.(=)
TNFRSF6B NM_003823.3 -?/. - c.-3562C>T r.(?) p.(=)
RTEL1 NM_016434.3 -?/. - c.2915C>T r.(?) p.(Thr972Ile)
RTEL1-TNFRSF6B NR_037882.1 -?/. - n.3742C>T r.(?) -


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