Variant #0000949049 (NC_000008.10:g.145740372C>G, NM_004260.3:c.1568G>C (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.145740372C>G
DNA change (hg38) -
Published as RECQL4(NM_004260.3):c.1568G>C (p.S523T)
ISCN -
DB-ID RECQL4_000036 See all 3 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) 0.00024 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC24 NM_001024678.3 ?/. - c.*7487G>C r.(=) p.(=)
RECQL4 NM_004260.3 ?/. - c.1568G>C r.(?) p.(Ser523Thr)
LRRC14 NM_014665.3 ?/. - c.-3165C>G r.(?) p.(=)
MFSD3 NM_138431.1 ?/. - c.*3825C>G r.(=) p.(=)


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