Variant #0000546295 (NC_000012.11:g.103352203_103352208dup, NM_004316.3:c.181_186dup (ASCL1))
| Chromosome |
12 |
| 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.103352203_103352208dup |
| DNA change (hg38) |
g.102958425_102958430dup |
| Published as |
ASCL1(NM_004316.3):c.181_186dupCAGCAG (p.Q61_Q62dup), PAH(NM_001354304.2):c.-300_-295dupTGCTGC |
| ISCN |
- |
| DB-ID |
ASCL1_000016 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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