Variant #0000332496 (NC_000008.10:g.145745747A>T, NM_004260.3:c.-2579T>A (RECQL4))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.145745747A>T
DNA change (hg38) g.144520363A>T
Published as LRRC14(NM_001272036.1):c.455A>T (p.(Gln152Leu))
ISCN -
DB-ID LRRC14_000002
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) 0.00227 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C8orf82 NM_001001795.1 ?/. - c.*6979T>A r.(=) p.(=)
LRRC24 NM_001024678.3 ?/. - c.*2112T>A r.(=) p.(=)
RECQL4 NM_004260.3 ?/. - c.-2579T>A r.(?) p.(=)
LRRC14 NM_014665.3 ?/. - c.455A>T r.(?) p.(Gln152Leu)


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