Variant #0000978136 (NC_000008.10:g.145738755_145738757dup, NM_004260.3:c.2308_2310dup (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.145738755_145738757dup
DNA change (hg38) -
Published as RECQL4(NM_004260.4):c.2307_2309dup (p.(Ala770dup))
ISCN -
DB-ID RECQL4_000302
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
LRRC24 NM_001024678.3 ?/. - c.*9102_*9104dup r.(=) p.(=)
RECQL4 NM_004260.3 ?/. - c.2308_2310dup r.? p.?
LRRC14 NM_014665.3 ?/. - c.-4782_-4780dup r.(?) p.(=)
MFSD3 NM_138431.1 ?/. - c.*2208_*2210dup r.(=) p.(=)


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