Variant #0000503782 (NC_000001.10:g.156124389G>A, NM_001193301.1:c.20G>A (SEMA4A))
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.156124389G>A |
DNA change (hg38) |
g.156154598G>A |
Published as |
SEMA4A(NM_022367.4):c.20G>A (p.G7D) |
ISCN |
- |
DB-ID |
SEMA4A_000035 |
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) |
0.00028 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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