Variant #0000291180 (NC_000008.10:g.145745829G>T, NM_004260.3:c.-2661C>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.145745829G>T
DNA change (hg38) g.144520445G>T
Published as LRRC14(NM_001272036.1):c.537G>T (p.A179=)
ISCN -
DB-ID LRRC14_000003
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-25 11:43:54 +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.*6897C>A r.(=) p.(=)
LRRC24 NM_001024678.3 -?/. - c.*2030C>A r.(=) p.(=)
RECQL4 NM_004260.3 -?/. - c.-2661C>A r.(?) p.(=)
LRRC14 NM_014665.3 -?/. - c.537G>T r.(?) p.(Ala179=)


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