Variant #0000328357 (NC_000020.10:g.32881908T>C, NM_000687.2:c.274A>G (AHCY))
Chromosome |
20 |
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.32881908T>C |
DNA change (hg38) |
g.34294102T>C |
Published as |
AHCY(NM_000687.2):c.274A>G (p.(Ile92Val)), AHCY(NM_001161766.2):c.190A>G (p.I64V), AHCY(NM_001322086.1):c.280A>G (p.I94V) |
ISCN |
- |
DB-ID |
AHCY_000003 See all 3 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) |
0.00341 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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