Variant #0001045867 (NC_000003.11:g.120369688C>T, NM_000187.3:c.367G>A (HGD))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.120369688C>T |
DNA change (hg38) |
- |
Published as |
HGD(NM_000187.3):c.367G>A (p.G123R), HGD(NM_000187.4):c.367G>A (p.G123R) |
ISCN |
- |
DB-ID |
HGD_000032 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) |
2.0E-5 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2025-07-08 13:22:38 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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