Variant #0000982138 (NC_000016.9:g.87637906_87637935dup, NC_000016.9(NM_020655.2):c.382+772_382+801dup (JPH3))
| Chromosome |
16 |
| 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.87637906_87637935dup |
| DNA change (hg38) |
- |
| Published as |
JPH3(NM_001271604.4):c.443_472dup (p.(Ala148_Ala157dup)) |
| ISCN |
- |
| DB-ID |
JPH3_000062 |
| 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 |
2024-04-19 20:27:30 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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