Variant #0000558389 (NC_000016.9:g.51174647dup, NM_002968.2:c.1488dup (SALL1))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.51174647dup |
DNA change (hg38) |
g.51140736dup |
Published as |
SALL1(NM_002968.2):c.1488dupT (p.Q497Sfs*19) |
ISCN |
- |
DB-ID |
SALL1_000065 |
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 |
2020-07-09 16:20:35 +02:00 (CEST) |

Variant on transcripts
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