Variant #0001065766 (NC_000012.11:g.56095165C>A, NC_000012.11(NM_002206.2):c.415-227G>T (ITGA7))
| Chromosome |
12 |
| 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.56095165C>A |
| DNA change (hg38) |
- |
| Published as |
ITGA7(NM_001144997.1):c.121G>T (p.(Glu41*)) |
| ISCN |
- |
| DB-ID |
ITGA7_000117 |
| 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) |
1.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2026-01-20 18:57:21 +01:00 (CET) |
| Date last edited |
2026-04-03 17:28:20 +02:00 (CEST) |

Variant on transcripts
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