Variant #0000344492 (NC_000020.10:g.62326110A>C, NM_016434.3:c.3126A>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.62326110A>C
DNA change (hg38) g.63694757A>C
Published as RTEL1(NM_001283009.1):c.3126A>C (p.Q1042H), RTEL1(NM_001283009.2):c.3126A>C (p.Q1042H)
ISCN -
DB-ID RTEL1-TNFRSF6B_000063 See all 3 reported entries
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) 0.75018 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZGPAT NM_001083113.1 -/. - c.-12830A>C r.(?) p.(=)
ARFRP1 NM_001134758.2 -/. - c.*5840T>G r.(=) p.(=)
TNFRSF6B NM_003823.3 -/. - c.-2011A>C r.(?) p.(=)
RTEL1 NM_016434.3 -/. - c.3126A>C r.(?) p.(Gln1042His)
RTEL1-TNFRSF6B NR_037882.1 -/. - n.3953A>C r.(?) -


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