Variant #0000611541 (NC_000008.10:g.145739029C>T, NM_004260.3:c.2126G>A (RECQL4))

Chromosome 8
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.145739029C>T
DNA change (hg38) g.144513645C>T
Published as RECQL4(NM_004260.3):c.2126G>A (p.R709Q)
ISCN -
DB-ID RECQL4_000222
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 2020-06-25 11:19:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC24 NM_001024678.3 ?/. - c.*8830G>A r.(=) p.(=)
RECQL4 NM_004260.3 ?/. - c.2126G>A r.(?) p.(Arg709Gln)
LRRC14 NM_014665.3 ?/. - c.-4508C>T r.(?) p.(=)
MFSD3 NM_138431.1 ?/. - c.*2482C>T r.(=) p.(=)


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