Variant #0000534343 (NC_000008.10:g.145740627C>T, NC_000008.10(NM_004260.3):c.1391-1G>A (RECQL4))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.145740627C>T
DNA change (hg38) g.144515243C>T
Published as -
ISCN -
DB-ID RECQL4_000037 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) 4.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-25 11:30:26 +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.*7232G>A r.(=) p.(=)
RECQL4 NM_004260.3 +/. - c.1391-1G>A r.spl? p.?
LRRC14 NM_014665.3 +/. - c.-2910C>T r.(?) p.(=)
MFSD3 NM_138431.1 +/. - c.*4080C>T r.(=) p.(=)


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