Variant #0000858676 (NC_000002.11:g.73646411A>C, NM_001378454.1:c.611A>C (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.73646411A>C |
DNA change (hg38) |
g.73419283A>C |
Published as |
ALMS1(NM_015120.4):c.614A>C (p.(Glu205Ala)) |
ISCN |
- |
DB-ID |
ALMS1_000797 |
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) |
0.0001 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|