Variant #0000573035 (NC_000023.10:g.110970141C>T, NM_001099922.2:c.1834C>T (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.110970141C>T |
| DNA change (hg38) |
g.111726913C>T |
| Published as |
ALG13(NM_001099922.2):c.1834C>T (p.(Pro612Ser)), ALG13(NM_001099922.3):c.1834C>T (p.P612S), ALG13(NM_001257231.1):c.1600C>T (p.P534S) |
| ISCN |
- |
| DB-ID |
ALG13_000007 See all 6 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) |
9.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2022-05-09 15:24:52 +02:00 (CEST) |

Variant on transcripts
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