Variant #0000570345 (NC_000020.10:g.62324601G>A, NM_016434.3:c.2957G>A (RTEL1))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.62324601G>A
DNA change (hg38) g.63693248G>A
Published as -
ISCN -
DB-ID ARFRP1_000036
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) 2.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 21:40:42 +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.*7349C>T r.(=) p.(=)
TNFRSF6B NM_003823.3 ?/. - c.-3520G>A r.(?) p.(=)
RTEL1 NM_016434.3 ?/. - c.2957G>A r.(?) p.(Arg986Gln)
RTEL1-TNFRSF6B NR_037882.1 ?/. - n.3784G>A r.(?) -


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