Variant #0000888243 (NC_000008.10:g.145739833A>G, NM_004260.3:c.1697T>C (RECQL4))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.145739833A>G
DNA change (hg38) -
Published as RECQL4(NM_004260.3):c.1697T>C (p.L566P), RECQL4(NM_004260.4):c.1697T>C (p.L566P)
ISCN -
DB-ID RECQL4_000035 See all 5 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) 0.00012 View details
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 2023-07-07 10:10:56 +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.*8026T>C r.(=) p.(=)
RECQL4 NM_004260.3 +?/. - c.1697T>C r.(?) p.(Leu566Pro)
LRRC14 NM_014665.3 +?/. - c.-3704A>G r.(?) p.(=)
MFSD3 NM_138431.1 +?/. - c.*3286A>G r.(=) p.(=)


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