Variant #0000534302 (NC_000008.10:g.145738527G>A, NC_000008.10(NM_004260.3):c.2464-6C>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.145738527G>A
DNA change (hg38) g.144513144G>A
Published as RECQL4(NM_004260.3):c.2464-6C>T
ISCN -
DB-ID RECQL4_000169
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC24 NM_001024678.3 -?/. - c.*9332C>T r.(=) p.(=)
RECQL4 NM_004260.3 -?/. - c.2464-6C>T r.(=) p.(=)
LRRC14 NM_014665.3 -?/. - c.-5010G>A r.(?) p.(=)
MFSD3 NM_138431.1 -?/. - c.*1980G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.