Variant #0000624190 (NC_000020.10:g.62311237C>T, NM_016434.3:c.1073C>T (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.62311237C>T
DNA change (hg38) g.63679884C>T
Published as RTEL1(NM_001283009.1):c.1073C>T (p.T358M)
ISCN -
DB-ID ARFRP1_000059
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-16 21:26:34 +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.*20713G>A r.(=) p.(=)
TNFRSF6B NM_003823.3 ?/. - c.-16884C>T r.(?) p.(=)
RTEL1 NM_016434.3 ?/. - c.1073C>T r.(?) p.(Thr358Met)
RTEL1-TNFRSF6B NR_037882.1 ?/. - n.1900C>T r.(?) -


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