Variant #0000656053 (NC_000008.10:g.145741168G>C, NM_004260.3:c.1238C>G (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.145741168G>C
DNA change (hg38) g.144515784G>C
Published as RECQL4(NM_004260.3):c.1238C>G (p.A413G, p.(Ala413Gly))
ISCN -
DB-ID RECQL4_000116 See all 3 reported entries
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) 0.00091 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-25 11:32:46 +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.*6691C>G r.(=) p.(=)
RECQL4 NM_004260.3 ?/. - c.1238C>G r.(?) p.(Ala413Gly)
LRRC14 NM_014665.3 ?/. - c.-2369G>C r.(?) p.(=)
MFSD3 NM_138431.1 ?/. - c.*4621G>C r.(=) p.(=)


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