Variant #0000808252 (NC_000017.10:g.73658944G>A, NM_004259.6:c.386C>T (RECQL5))

Chromosome 17
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.73658944G>A
DNA change (hg38) -
Published as RECQL5(NM_004259.6):c.386C>T (p.T129I)
ISCN -
DB-ID RECQL5_000075
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMIM5 NM_001162995.2 ?/. - c.*21967G>A r.(=) p.(=)
SMIM6 NM_001162997.1 ?/. - c.*15299G>A r.(=) p.(=)
RECQL5 NM_004259.6 ?/. - c.386C>T r.(?) p.(Thr129Ile)
SAP30BP NM_013260.6 ?/. - c.-4509G>A r.(?) p.(=)


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