Variant #0000890479 (NC_000012.11:g.21623299_21623300dup, NC_000012.11(NM_002907.3):c.1798-6_1798-5dup (RECQL))

Chromosome 12
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.21623299_21623300dup
DNA change (hg38) -
Published as RECQL(NM_002907.3):c.1798-6_1798-5insTT (p.?), RECQL(NM_002907.4):c.1798-6_1798-5dupTT
ISCN -
DB-ID PYROXD1_000020 See all 2 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RECQL NM_002907.3 -/. - c.1798-6_1798-5dup r.spl? p.?
PYROXD1 NM_024854.3 -/. - c.*1611_*1612dup r.(=) p.(=)


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