Variant #0000618294 (NC_000020.10:g.62292835_62292837dup, NM_016434.3:c.287_289dup (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.62292835_62292837dup
DNA change (hg38) g.63661482_63661484dup
Published as RTEL1(NM_001283009.1):c.287_289dupCTG (p.A96dup)
ISCN -
DB-ID ARFRP1_000055
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARFRP1 NM_001134758.2 ?/. - c.*39126_*39128dup r.(=) p.(=)
TNFRSF6B NM_003823.3 ?/. - c.-35286_-35284dup r.(?) p.(=)
RTEL1 NM_016434.3 ?/. - c.287_289dup r.(?) p.(Ala96dup)
RTEL1-TNFRSF6B NR_037882.1 ?/. - n.1114_1116dup r.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.