Variant #0000547457 (NC_000012.11:g.21623294_21623300dup, NC_000012.11(NM_002907.3):c.1798-11_1798-5dup (RECQL))

Chromosome 12
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.21623294_21623300dup
DNA change (hg38) g.21470360_21470366dup
Published as RECQL(NM_002907.3):c.1798-5_1798-4insTTTTTTT (p.?)
ISCN -
DB-ID PYROXD1_000015
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_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 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RECQL NM_002907.3 -?/. - c.1798-11_1798-5dup r.spl? p.?
PYROXD1 NM_024854.3 -?/. - c.*1606_*1612dup r.(=) p.(=)


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