Variant #0000037918 (NC_000019.9:g.18709768G>A, NC_000019.9(NM_004750.4):c.398-57C>T (CRLF1))
| Chromosome |
19 |
| 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.18709768G>A |
| DNA change (hg38) |
g.18598958G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CRLF1_000041 |
| Variant remarks |
- |
| Reference |
PubMed: Piras 2014 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2014-06-27 20:03:51 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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