Variant #0000848757 (NC_000001.10:g.45974622G>C, NM_015506.2:c.584G>C (MMACHC))
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.45974622G>C |
DNA change (hg38) |
- |
Published as |
MMACHC(NM_001330540.1):c.413G>C (p.(Gly138Ala)), MMACHC(NM_015506.2):c.584G>C (p.G195A) |
ISCN |
- |
DB-ID |
MMACHC_000045 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) |
5.0E-5 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 15:40:45 +02:00 (CEST) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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