Variant #0000367750 (NC_000013.10:g.101735211G>A, NM_052867.2:c.3714C>T (NALCN))
| Individual ID |
00163650 |
| Chromosome |
13 |
| 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.101735211G>A |
| DNA change (hg38) |
g.101082860G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
NALCN_000022 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs17677552 |
| Origin |
Unknown |
| Segregation |
? |
| Frequency |
0.37 controls |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.35142 View details |
| Owner |
Florian Erger |
| Database submission license |
No license selected |
| Created by |
Florian Erger |
| Date created |
2018-04-03 17:38:28 +02:00 (CEST) |
| Date last edited |
2018-04-06 09:40:51 +02:00 (CEST) |

Variant on transcripts
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