Variant #0000570364 (NC_000020.10:g.62329785C>T, NM_016434.3:c.*2647C>T (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.62329785C>T
DNA change (hg38) g.63698432C>T
Published as TNFRSF6B(NM_003823.3):c.772C>T (p.(Arg258Cys))
ISCN -
DB-ID ARFRP1_000051
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) 0.00012 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 21:49:26 +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.-9155C>T r.(?) p.(=)
ARFRP1 NM_001134758.2 -?/. - c.*2165G>A r.(=) p.(=)
TNFRSF6B NM_003823.3 -?/. - c.772C>T r.(?) p.(Arg258Cys)
RTEL1 NM_016434.3 -?/. - c.*2647C>T r.(=) p.(=)
RTEL1-TNFRSF6B NR_037882.1 -?/. - n.5506C>T r.(?) -


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