Variant #0000659516 (NC_000019.9:g.18710546A>G, NM_004750.4:c.226T>C (CRLF1))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.18710546A>G |
| DNA change (hg38) |
g.18599736A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CRLF1_000051 |
| Variant remarks |
- |
| Reference |
{Buers 2020: 31497877} |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Insa Buers |
| Database submission license |
No license selected |
| Created by |
Insa Buers |
| Date created |
2020-03-24 13:43:57 +01:00 (CET) |
| Date last edited |
2020-07-15 16:10:09 +02:00 (CEST) |

Variant on transcripts
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