Variant #0000655713 (NC_000007.13:g.116339121G>A, NC_000007.13(NM_001127500.1):c.-14-4G>A (MET))
| Chromosome |
7 |
| 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.116339121G>A |
| DNA change (hg38) |
g.116699067G>A |
| Published as |
MET(NM_000245.4):c.-14-4G>A, MET(NM_001127500.1):c.-14-4G>A |
| ISCN |
- |
| DB-ID |
MET_000166 See all 2 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) |
0.00079 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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