Variant #0000866588 (NC_000020.10:g.62305406T>C, NM_016434.3:c.879T>C (RTEL1))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.62305406T>C
DNA change (hg38) -
Published as RTEL1(NM_016434.3):c.879T>C (p.(=))
ISCN -
DB-ID ARFRP1_000092
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) 0.0137 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 2023-01-11 15:44:22 +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.*26544A>G r.(=) p.(=)
TNFRSF6B NM_003823.3 -/. - c.-22715T>C r.(?) p.(=)
RTEL1 NM_016434.3 -/. - c.879T>C r.(?) p.(Gly293=)
RTEL1-TNFRSF6B NR_037882.1 -/. - n.1706T>C r.(?) -


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