Variant #0000570359 (NC_000020.10:g.62326910G>A, NC_000020.10(NM_016434.3):c.3652+77G>A (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.62326910G>A
DNA change (hg38) g.63695557G>A
Published as RTEL1(NM_001283009.1):c.3729G>A (p.V1243=)
ISCN -
DB-ID ARFRP1_000047
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 21:46:57 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZGPAT NM_001083113.1 -?/. - c.-12030G>A r.(?) p.(=)
ARFRP1 NM_001134758.2 -?/. - c.*5040C>T r.(=) p.(=)
TNFRSF6B NM_003823.3 -?/. - c.-1211G>A r.(?) p.(=)
RTEL1 NM_016434.3 -?/. - c.3652+77G>A r.(=) p.(=)
RTEL1-TNFRSF6B NR_037882.1 -?/. - n.4556G>A r.(?) -


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