Variant #0000548957 (NC_000012.11:g.64491020G>T, NC_000012.11(NM_020762.2):c.1679-1G>T (SRGAP1))
| Chromosome |
12 |
| 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.64491020G>T |
| DNA change (hg38) |
g.64097240G>T |
| Published as |
SRGAP1(NM_020762.2):c.1679-1G>T (p.?) |
| ISCN |
- |
| DB-ID |
SRGAP1_000005 |
| 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) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-07-02 16:54:13 +02:00 (CEST) |

Variant on transcripts
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