Variant #0000803564 (NC_000008.10:g.145743140C>T, NM_004260.3:c.29G>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.145743140C>T
DNA change (hg38) -
Published as RECQL4(NM_004260.3):c.29G>A (p.R10Q), RECQL4(NM_004260.4):c.29G>A (p.(Arg10Gln))
ISCN -
DB-ID RECQL4_000264 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C8orf82 NM_001001795.1 ?/. - c.*9586G>A r.(=) p.(=)
LRRC24 NM_001024678.3 ?/. - c.*4719G>A r.(=) p.(=)
RECQL4 NM_004260.3 ?/. - c.29G>A r.(?) p.(Arg10Gln)
LRRC14 NM_014665.3 ?/. - c.-397C>T r.(?) p.(=)


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