Variant #0000722834 (NC_000010.10:g.50856559G>A, NM_020549.4:c.1288G>A (CHAT))
| Chromosome |
10 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.50856559G>A |
| DNA change (hg38) |
- |
| Published as |
CHAT(NM_001142933.2):c.1042G>A (p.V348M), CHAT(NM_020549.5):c.1288G>A (p.(Val430Met)) |
| ISCN |
- |
| DB-ID |
CHAT_000060 See all 4 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) |
2.0E-5 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2021-02-08 18:36:18 +01:00 (CET) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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