Variant #0000544934 (NC_000011.9:g.64575505C>T, NM_004579.3:c.-4884G>A (MAP4K2))
| Chromosome |
11 |
| 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.64575505C>T |
| DNA change (hg38) |
g.64808033C>T |
| Published as |
MEN1(NM_000244.3):c.527G>A (p.(Arg176Gln), p.R176Q), MEN1(NM_130803.2):c.527G>A (p.R176Q), MEN1(NM_130803.3):c.527G>A (p.R176Q) |
| ISCN |
- |
| DB-ID |
MEN1_000064 See all 9 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) |
0.01202 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-11-27 17:27:23 +01:00 (CET) |

Variant on transcripts
|