Variant #0000405583 (NC_000004.11:g.72215736A>G, NM_001098484.2:c.497A>G (SLC4A4))
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.72215736A>G |
| DNA change (hg38) |
g.71350019A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SLC4A4_000012 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Yamazaki 2011 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Mark Parker |
| Database submission license |
No license selected |
| Created by |
Mark Parker |
| Date created |
2012-05-18 20:09:40 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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