Variant #0000618295 (NC_000020.10:g.62292841A>C, NM_016434.3:c.293A>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.62292841A>C
DNA change (hg38) g.63661488A>C
Published as RTEL1(NM_001283009.1):c.293A>C (p.D98A)
ISCN -
DB-ID ARFRP1_000056
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-16 21:21:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARFRP1 NM_001134758.2 -?/. - c.*39109T>G r.(=) p.(=)
TNFRSF6B NM_003823.3 -?/. - c.-35280A>C r.(?) p.(=)
RTEL1 NM_016434.3 -?/. - c.293A>C r.(?) p.(Asp98Ala)
RTEL1-TNFRSF6B NR_037882.1 -?/. - n.1120A>C r.(?) -


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