Variant #0000540452 (NC_000010.10:g.69959174C>T, NM_032578.3:c.3335C>T (MYPN))
| Chromosome |
10 |
| 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.69959174C>T |
| DNA change (hg38) |
g.68199417C>T |
| Published as |
MYPN(NM_001256267.1):c.3335C>T (p.P1112L), MYPN(NM_001256268.2):c.2453C>T (p.P818L), MYPN(NM_032578.3):c.3335C>T (p.P1112L), MYPN(NM_032578.4):c.33... |
| ISCN |
- |
| DB-ID |
MYPN_000003 See all 11 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) |
0.00319 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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