Variant #0000609718 (NC_000005.9:g.37310678G>A, NM_153485.1:c.2604C>T (NUP155))
| Chromosome |
5 |
| 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.37310678G>A |
| DNA change (hg38) |
g.37310576G>A |
| Published as |
NUP155(NM_004298.3):c.2427C>T (p.S809=) |
| ISCN |
- |
| DB-ID |
NUP155_000002 |
| 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 |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2020-06-17 10:05:41 +02:00 (CEST) |

Variant on transcripts
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