Variant #0000545599 (NC_000011.9:g.70338541T>G, NM_012309.4:c.2191A>C (SHANK2))
| Chromosome |
11 |
| 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.70338541T>G |
| DNA change (hg38) |
g.70490371T>G |
| Published as |
SHANK2(NM_012309.3):c.2192A>C (p.(Lys780Gln)), SHANK2(NM_133266.3):c.574A>C (p.K192Q) |
| ISCN |
- |
| DB-ID |
SHANK2_000022 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) |
0.00083 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 |
2020-08-06 14:59:34 +02:00 (CEST) |

Variant on transcripts
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