Variant #0000532720 (NC_000007.13:g.81392140G>A, NM_000601.4:c.137C>T (HGF))
| 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.81392140G>A |
| DNA change (hg38) |
g.81762824G>A |
| Published as |
HGF(NM_000601.4):c.137C>T (p.(Ala46Val)), HGF(NM_000601.5):c.137C>T (p.A46V), HGF(NM_000601.6):c.137C>T (p.A46V) |
| ISCN |
- |
| DB-ID |
HGF_000015 See all 3 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) |
0.00177 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 |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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