Variant #0000547461 (NC_000012.11:g.21623298_21623300dup, NC_000012.11(NM_002907.3):c.1798-7_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.21623298_21623300dup
DNA change (hg38) g.21470364_21470366dup
Published as RECQL(NM_002907.3):c.1798-5_1798-4insTTT (p.?)
ISCN -
DB-ID PYROXD1_000019
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 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RECQL NM_002907.3 -?/. - c.1798-7_1798-5dup r.spl? p.?
PYROXD1 NM_024854.3 -?/. - c.*1610_*1612dup r.(=) p.(=)


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