Variant #0000870310 (NC_000002.11:g.29296355C>A, NM_001029883.2:c.773G>T (C2orf71))
| Chromosome |
2 |
| 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.29296355C>A |
| DNA change (hg38) |
- |
| Published as |
c.773G>T |
| ISCN |
- |
| DB-ID |
C2orf71_000210 |
| Variant remarks |
- |
| Reference |
PubMed: Audo 2011 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
? |
| Frequency |
1/418 patient chromosomes; 0/190 control chromosomes |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00238 View details |
| Owner |
LOVD |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2022-06-18 03:05:08 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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