Variant #0000576556 (NC_000023.10:g.53227066_53227068dup, KDM5C(NM_004187.3):c.2517-9_2517-7dup)

Chromosome X
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.53227066_53227068dup
DNA change (hg38) g.53197884_53197886dup
Published as KDM5C(NM_001146702.1):c.2316-7_2316-6insACT (p.(=)), KDM5C(NM_004187.4):c.2517-11_2517-10insTAC, KDM5C(NM_004187.4):c.2517-9_2517-7dupACT
ISCN -
DB-ID KDM5C_000087 See all 3 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) Variant not found in online data sets
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KDM5C NM_004187.3 -?/. - c.2517-9_2517-7dup r.(=) p.(=)