Variant #0000299303 (NC_000008.10:g.145741783T>G, NM_004260.3:c.720A>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.145741783T>G
DNA change (hg38) g.144516399T>G
Published as RECQL4(NM_004260.3):c.720A>C (p.S240=), RECQL4(NM_004260.4):c.720A>C (p.S240=)
ISCN -
DB-ID RECQL4_000124 See all 2 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +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.*6076A>C r.(=) p.(=)
RECQL4 NM_004260.3 -?/. - c.720A>C r.(?) p.(Ser240=)
LRRC14 NM_014665.3 -?/. - c.-1754T>G r.(?) p.(=)


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