Variant #0000268089 (NC_000019.9:g.33792900C>A, CEBPA(NM_004364.3):c.421G>T)
Chromosome |
19 |
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.33792900C>A |
DNA change (hg38) |
g.33301994C>A |
Published as |
CEBPA(NM_001285829.1):c.64G>T (p.G22C), CEBPA(NM_004364.3):c.421G>T (p.G141C) |
ISCN |
- |
DB-ID |
CEBPA_000008 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 |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
VKGL-NL_VUmc |

Variant on transcripts
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