Variant #0000534372 (NC_000008.10:g.145743149A>C, NM_004260.3:c.20T>G (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.145743149A>C
DNA change (hg38) g.144517765A>C
Published as RECQL4(NM_004260.3):c.20T>G (p.(Val7Gly), p.V7G)
ISCN -
DB-ID RECQL4_000210 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) 0.00011 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 2022-05-09 15:24:52 +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.*9577T>G r.(=) p.(=)
LRRC24 NM_001024678.3 -?/. - c.*4710T>G r.(=) p.(=)
RECQL4 NM_004260.3 -?/. - c.20T>G r.(?) p.(Val7Gly)
LRRC14 NM_014665.3 -?/. - c.-388A>C r.(?) p.(=)


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