Variant #0000534315 (NC_000008.10:g.145738669C>T, NM_004260.3:c.2395G>A (RECQL4))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145738669C>T
DNA change (hg38) g.144513286C>T
Published as RECQL4(NM_004260.3):c.2395G>A (p.(Val799Met), p.V799M), RECQL4(NM_004260.4):c.2395G>A (p.V799M)
ISCN -
DB-ID RECQL4_000090 See all 6 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) 0.01603 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC24 NM_001024678.3 -?/. - c.*9190G>A r.(=) p.(=)
RECQL4 NM_004260.3 -?/. - c.2395G>A r.(?) p.(Val799Met)
LRRC14 NM_014665.3 -?/. - c.-4868C>T r.(?) p.(=)
MFSD3 NM_138431.1 -?/. - c.*2122C>T r.(=) p.(=)


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