Variant #0000534298 (NC_000008.10:g.145738375C>G, NM_004260.3:c.2610G>C (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.145738375C>G
DNA change (hg38) g.144512992C>G
Published as RECQL4(NM_004260.3):c.2611G>C (p.(Gly871Arg))
ISCN -
DB-ID RECQL4_000166
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.*9484G>C r.(=) p.(=)
RECQL4 NM_004260.3 -?/. - c.2610G>C r.(?) p.(Gly870=)
LRRC14 NM_014665.3 -?/. - c.-5162C>G r.(?) p.(=)
MFSD3 NM_138431.1 -?/. - c.*1828C>G r.(=) p.(=)


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