Variant #0000570298 (NC_000020.10:g.62289614G>C, NM_016434.3:c.-376G>C (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.62289614G>C
DNA change (hg38) g.63658261G>C
Published as RTEL1(NM_001283009.1):c.-376G>C
ISCN -
DB-ID ARFRP1_000001
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 2021-09-17 14:40:49 +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.*42336C>G r.(=) p.(=)
TNFRSF6B NM_003823.3 -/. - c.-38507G>C r.(?) p.(=)
STMN3 NM_015894.2 -/. - c.-4916C>G r.(?) p.(=)
RTEL1 NM_016434.3 -/. - c.-376G>C r.(?) p.(=)
RTEL1-TNFRSF6B NR_037882.1 -/. - n.452G>C r.(?) -


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