Variant #0000656323 (NC_000009.11:g.2039795_2039796insCGC, NM_003070.3:c.685_686insCGC (SMARCA2))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2039795_2039796insCGC |
| DNA change (hg38) |
g.2039795_2039796insCGC |
| Published as |
SMARCA2(NM_003070.4):c.685_686insCGC (p.Q228_Q229insP), SMARCA2(NM_003070.5):c.685_686insCGC (p.(Gln228_Gln229insPro)), SMARCA2(NM_003070.5):c.685_... |
| ISCN |
- |
| DB-ID |
SMARCA2_000119 See all 3 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) |
Retrieve |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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