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
|