Variant #0000922924 (NC_000001.10:g.11907430T>G, NM_005957.4:c.-41499A>C (MTHFR))
| Chromosome |
1 |
| 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.11907430T>G |
| DNA change (hg38) |
- |
| Published as |
NPPA(NM_006172.3):c.190A>C (p.S64R, p.(Ser64Arg)), NPPA(NM_006172.4):c.190A>C (p.S64R), NPPA-AS1(NR_037806.1):n.1480-61T>G |
| ISCN |
- |
| DB-ID |
NPPA_000006 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) |
0.00198 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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