Variant #0000086602 (NC_000007.13:g.138417718A>G, NM_020632.2:c.1812T>C (ATP6V0A4))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.138417718A>G |
| DNA change (hg38) |
g.138732973A>G |
| Published as |
C>T (H604H) |
| ISCN |
- |
| DB-ID |
ATP6V0A4_000010 See all 3 reported entries |
| Variant remarks |
ethnically matched controls |
| Reference |
PubMed: Smith 2000, Journal: Smith 2000 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.68 controls |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.72917 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2015-12-18 13:35:01 +01:00 (CET) |
| Date last edited |
2019-04-09 14:57:52 +02:00 (CEST) |

Variant on transcripts
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