Variant #0000659045 (NC_000023.10:g.110988098T>C, NM_001099922.2:c.2898T>C (ALG13))
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.110988098T>C |
DNA change (hg38) |
g.111744870T>C |
Published as |
ALG13(NM_001257231.1):c.2664T>C (p.Y888=) |
ISCN |
- |
DB-ID |
ALG13_000064 See all 2 reported entries |
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) |
0.00081 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2020-07-21 08:56:33 +02:00 (CEST) |

Variant on transcripts
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