Variant #0000545638 (NC_000011.9:g.71717267A>G, NM_001145309.3:c.-75207A>G (LRTOMT))
| Chromosome |
11 |
| 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.71717267A>G |
| DNA change (hg38) |
g.72006221A>G |
| Published as |
NUMA1(NM_001286561.1):c.5464T>C (p.Y1822H), NUMA1(NM_006185.2):c.5506T>C (p.(Tyr1836His)) |
| ISCN |
- |
| DB-ID |
NUMA1_000001 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) |
0.00543 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
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