Variant #0000617473 (NC_000019.9:g.18979423C>T, NM_001492.4:c.1102G>A (GDF1))
Chromosome |
19 |
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.18979423C>T |
DNA change (hg38) |
g.18868614C>T |
Published as |
GDF1(NM_001492.6):c.1102G>A (p.E368K) |
ISCN |
- |
DB-ID |
GDF1_000041 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) |
7.0E-5 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
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