Variant #0000849996 (NC_000002.11:g.73675553A>G, NM_001378454.1:c.1899A>G (ALMS1))
Chromosome |
2 |
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.73675553A>G |
DNA change (hg38) |
g.73448426A>G |
Published as |
ALMS1(NM_015120.4):c.1902A>G (p.Q634=) |
ISCN |
- |
DB-ID |
ALMS1_000799 |
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) |
0.00304 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-05-09 15:40:45 +02:00 (CEST) |
Date last edited |
2024-05-17 21:20:31 +02:00 (CEST) |

Variant on transcripts
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