Variant #0000534356 (NC_000008.10:g.145741432G>A, NM_004260.3:c.1071C>T (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.145741432G>A
DNA change (hg38) g.144516048G>A
Published as RECQL4(NM_004260.3):c.1071C>T (p.N357=)
ISCN -
DB-ID RECQL4_000199
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-25 11:35:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC24 NM_001024678.3 -?/. - c.*6427C>T r.(=) p.(=)
RECQL4 NM_004260.3 -?/. - c.1071C>T r.(?) p.(Asn357=)
LRRC14 NM_014665.3 -?/. - c.-2105G>A r.(?) p.(=)
MFSD3 NM_138431.1 -?/. - c.*4885G>A r.(=) p.(=)


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