Variant #0000614431 (NC_000012.11:g.9085340_9085342dup, NM_001207024.1:c.*9087_*9089dup (M6PR))
| Chromosome |
12 |
| 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.9085340_9085342dup |
| DNA change (hg38) |
g.8932744_8932746dup |
| Published as |
PHC1(NM_004426.2):c.1271_1272insGCA (p.(Ala424_Gln425insGln)), PHC1(NM_004426.2):c.1287_1289dupGCA (p.Q439dup) |
| ISCN |
- |
| DB-ID |
M6PR_000003 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 |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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