Variant #0000895431 (NC_000020.10:g.62316867del, NC_000020.10(NM_016434.3):c.1192-9del (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.62316867del
DNA change (hg38) -
Published as RTEL1(NM_001283010.1):c.523-9delG
ISCN -
DB-ID ARFRP1_000099
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) 0.00249 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.*15083del r.(?) p.(=)
TNFRSF6B NM_003823.3 -/. - c.-11254del r.(?) p.(=)
RTEL1 NM_016434.3 -/. - c.1192-9del r.(=) p.(=)
RTEL1-TNFRSF6B NR_037882.1 -/. - n.2019-9del r.(?) -


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