Variant #0000507698 (NC_000001.10:g.45973127C>T, NM_015506.2:c.181C>T (MMACHC))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45973127C>T |
DNA change (hg38) |
g.45507455C>T |
Published as |
MMACHC(NM_001330540.1):c.10C>T (p.R4W, p.(Arg4Trp)), MMACHC(NM_001330540.2):c.10C>T (p.R4W), MMACHC(NM_015506.3):c.181C>T (p.R61W) |
ISCN |
- |
DB-ID |
MMACHC_000005 See all 4 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) |
0.00058 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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