Variant #0000611546 (NC_000008.10:g.145741455T>C, NM_004260.3:c.1048A>G (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.145741455T>C
DNA change (hg38) g.144516071T>C
Published as RECQL4(NM_004260.3):c.1048A>G (p.R350G)
ISCN -
DB-ID RECQL4_000225
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) 1.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-25 11:36:17 +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.*6404A>G r.(=) p.(=)
RECQL4 NM_004260.3 -?/. - c.1048A>G r.(?) p.(Arg350Gly)
LRRC14 NM_014665.3 -?/. - c.-2082T>C r.(?) p.(=)
MFSD3 NM_138431.1 -?/. - c.*4908T>C r.(=) p.(=)


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