Variant #0000856904 (NC_000001.10:g.11854476T>G, NM_005957.4:c.1286A>C (MTHFR))
| Chromosome |
1 |
| 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.11854476T>G |
| DNA change (hg38) |
- |
| Published as |
MTHFR(NM_001330358.1):c.1409A>C (p.E470A), MTHFR(NM_005957.4):c.1286A>C (p.E429A), MTHFR(NM_005957.5):c.1286A>C (p.E429A, p.(Glu429Ala)) |
| ISCN |
- |
| DB-ID |
MTHFR_000016 See all 6 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) |
0.29019 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
| Date last edited |
2024-04-19 20:20:39 +02:00 (CEST) |

Variant on transcripts
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