Variant #0000506099 (NC_000001.10:g.235971751A>G, NC_000001.10(NM_000081.3):c.2363+4T>C (LYST))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.235971751A>G |
| DNA change (hg38) |
g.235808451A>G |
| Published as |
LYST(NM_000081.2):c.2363+4T>C (p.?), LYST(NM_000081.3):c.2363+4T>C, LYST(NM_001301365.1):c.2363+4T>C |
| ISCN |
- |
| DB-ID |
LYST_000070 See all 4 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) |
0.00136 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 |
2020-06-05 20:32:03 +02:00 (CEST) |

Variant on transcripts
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