Variant #0000282473 (NC_000011.9:g.64572560C>T, NM_004579.3:c.-1939G>A (MAP4K2))
| 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.64572560C>T |
| DNA change (hg38) |
g.64805088C>T |
| Published as |
MEN1(NM_000244.3):c.1311G>A (p.L437=), MEN1(NM_130799.2):c.1296G>A (p.L432=), MEN1(NM_130803.2):c.1311G>A (p.L437=), MEN1(NM_130803.3):c.1311G>A ...) |
| ISCN |
- |
| DB-ID |
MEN1_000014 See all 5 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) |
0.00113 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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