Variant #0000291753 (NC_000007.13:g.116339642G>T, NM_001127500.1:c.504G>T (MET))
Chromosome |
7 |
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.116339642G>T |
DNA change (hg38) |
g.116699588G>T |
Published as |
MET(NM_000245.2):c.504G>T (p.(Glu168Asp)), MET(NM_000245.4):c.504G>T (p.E168D), MET(NM_001127500.1):c.504G>T (p.E168D), MET(NM_001127500.3):c.504G>... |
ISCN |
- |
DB-ID |
MET_000121 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) |
0.00369 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
|