Variant #0000299300 (NC_000008.10:g.145742011C>T, NM_004260.3:c.492G>A (RECQL4))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145742011C>T
DNA change (hg38) g.144516627C>T
Published as RECQL4(NM_004260.4):c.492G>A (p.E164=)
ISCN -
DB-ID RECQL4_000128
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) 0.0086 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.*5848G>A r.(=) p.(=)
RECQL4 NM_004260.3 -/. - c.492G>A r.(?) p.(Glu164=)
LRRC14 NM_014665.3 -/. - c.-1526C>T r.(?) p.(=)


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