Variant #0000915434 (NC_000020.10:g.62327126C>G, NC_000020.10(NM_016434.3):c.3653-5C>G (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.62327126C>G
DNA change (hg38) -
Published as RTEL1(NM_001283009.1):c.3823-5C>G, RTEL1(NM_001283010.1):c.2984-5C>G, RTEL1(NM_016434.3):c.3653-5C>G (p.?)
ISCN -
DB-ID RTEL1-TNFRSF6B_000032 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) 0.00273 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 2023-01-11 15:44:22 +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     
ZGPAT NM_001083113.1 -?/. - c.-11814C>G r.(?) p.(=)
ARFRP1 NM_001134758.2 -?/. - c.*4824G>C r.(=) p.(=)
TNFRSF6B NM_003823.3 -?/. - c.-995C>G r.(?) p.(=)
RTEL1 NM_016434.3 -?/. - c.3653-5C>G r.spl? p.?
RTEL1-TNFRSF6B NR_037882.1 -?/. - n.4650-5C>G r.(?) -


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