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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