Variant #0000307418 (NC_000020.10:g.62326873C>T, NC_000020.10(NM_016434.3):c.3652+40C>T (RTEL1))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.62326873C>T
DNA change (hg38) g.63695520C>T
Published as RTEL1(NM_001283009.1):c.3692C>T (p.T1231M)
ISCN -
DB-ID RTEL1-TNFRSF6B_000030
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) 0.00126 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-16 21:46:38 +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.-12067C>T r.(?) p.(=)
ARFRP1 NM_001134758.2 -/. - c.*5077G>A r.(=) p.(=)
TNFRSF6B NM_003823.3 -/. - c.-1248C>T r.(?) p.(=)
RTEL1 NM_016434.3 -/. - c.3652+40C>T r.(=) p.(=)
RTEL1-TNFRSF6B NR_037882.1 -/. - n.4519C>T r.(?) -


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