Variant #0000259553 (NC_000019.9:g.42492088G>A, ATP1A3(NM_152296.4):c.357C>T)
Chromosome |
19 |
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.42492088G>A |
DNA change (hg38) |
g.41987936G>A |
Published as |
ATP1A3(NM_001256213.1):c.390C>T (p.(Asn130=)), ATP1A3(NM_001256214.1):c.396C>T (p.N132=), ATP1A3(NM_001256214.2):c.396C>T (p.N132=) |
ISCN |
- |
DB-ID |
ATP1A3_000072 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) |
0.00244 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |

Variant on transcripts
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