Variant #0000711813 (NC_000006.11:g.42666061T>C, NM_000322.4:c.1013A>G (PRPH2))
| Chromosome |
6 |
| Allele |
Parent #1 |
| 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.42666061T>C |
| DNA change (hg38) |
- |
| Published as |
1014G>A (GGC?GAC) Gly338Asp |
| ISCN |
- |
| DB-ID |
PRPH2_000003 See all 16 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Sohocki 2001 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
0.22 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.77653 View details |
| Owner |
Julia Lopez |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2021-01-14 12:40:33 +01:00 (CET) |
| Date last edited |
2021-10-29 16:57:32 +02:00 (CEST) |

Variant on transcripts
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