Variant #0000521136 (NC_000004.11:g.1087327_1087328insCTGCCCAGGCTGGAGCCAGCC, NC_000004.11(NM_194439.4):c.247-2702_247-2701insGGCTGGCTCCAGCCTGGGCAG (RNF212))
| Chromosome |
4 |
| 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.1087327_1087328insCTGCCCAGGCTGGAGCCAGCC |
| DNA change (hg38) |
g.1093539_1093540insCTGCCCAGGCTGGAGCCAGCC |
| Published as |
RNF212(NM_001193318.2):c.721_722insGGCTGGCTCCAGCCTGGGCAG (p.S241delins8) |
| ISCN |
- |
| DB-ID |
RNF212_000007 |
| 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_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 |
2022-05-09 15:24:52 +02:00 (CEST) |

Variant on transcripts
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