Variant #0000619688 (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_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |

Variant on transcripts
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