Variant #0000297631 (NC_000008.10:g.145741702C>G, NM_004260.3:c.801G>C (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.145741702C>G
DNA change (hg38) g.144516318C>G
Published as RECQL4(NM_004260.4):c.801G>C (p.E267D)
ISCN -
DB-ID RECQL4_000122 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) 0.43745 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.*6157G>C r.(=) p.(=)
RECQL4 NM_004260.3 -/. - c.801G>C r.(?) p.(Glu267Asp)
LRRC14 NM_014665.3 -/. - c.-1835C>G r.(?) p.(=)


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