Variant #0000929427 (NC_000008.10:g.145739069G>A, NM_004260.3:c.2086C>T (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.145739069G>A
DNA change (hg38) -
Published as RECQL4(NM_004260.3):c.2086C>T (p.R696C, p.(Arg696Cys))
ISCN -
DB-ID RECQL4_000096 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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-07-07 10:10:56 +02:00 (CEST)
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.*8790C>T r.(=) p.(=)
RECQL4 NM_004260.3 ?/. - c.2086C>T r.(?) p.(Arg696Cys)
LRRC14 NM_014665.3 ?/. - c.-4468G>A r.(?) p.(=)
MFSD3 NM_138431.1 ?/. - c.*2522G>A r.(=) p.(=)


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