Variant #0000534352 (NC_000008.10:g.145741236A>G, NM_004260.3:c.1170T>C (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.145741236A>G
DNA change (hg38) g.144515852A>G
Published as -
ISCN -
DB-ID RECQL4_000195
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) 0.00015 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-25 11:33:44 +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.*6623T>C r.(=) p.(=)
RECQL4 NM_004260.3 ?/. - c.1170T>C r.(?) p.(Phe390=)
LRRC14 NM_014665.3 ?/. - c.-2301A>G r.(?) p.(=)
MFSD3 NM_138431.1 ?/. - c.*4689A>G r.(=) p.(=)


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