Variant #0001027190 (NC_000019.9:g.17039023A>C, NM_015692.2:c.3307T>G (CPAMD8))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.17039023A>C |
| DNA change (hg38) |
- |
| Published as |
CPAMD8(NM_015692.5):c.3166T>G (p.S1056A) |
| ISCN |
- |
| DB-ID |
CPAMD8_000057 |
| 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) |
0.00906 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2025-02-07 18:57:27 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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