Variant #0000619416 (NC_000023.10:g.23398373T>C, NC_000023.10(NM_173495.2):c.1012+5T>C (PTCHD1))
| 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.23398373T>C |
| DNA change (hg38) |
g.23380256T>C |
| Published as |
PTCHD1(NM_173495.2):c.1012+5T>C (p.?), PTCHD1(NM_173495.3):c.1012+5T>C |
| ISCN |
- |
| DB-ID |
PTCHD1_000039 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) |
0.00041 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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