Variant #0000656446 (NC_000010.10:g.127462710G>T, NM_147191.1:c.387C>A (MMP21))
Chromosome |
10 |
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.127462710G>T |
DNA change (hg38) |
g.125774141G>T |
Published as |
MMP21(NM_147191.1):c.387C>A (p.A129=) |
ISCN |
- |
DB-ID |
MMP21_000032 |
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) |
0.00388 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2020-06-29 11:27:23 +02:00 (CEST) |

Variant on transcripts
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