Variant #0000889071 (NC_000010.10:g.13325784C>T, NM_006214.3:c.734G>A (PHYH))
Chromosome |
10 |
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.13325784C>T |
DNA change (hg38) |
- |
Published as |
PHYH(NM_001037537.2):c.434G>A (p.R145Q), PHYH(NM_001323080.2):c.434G>A (p.R145Q), PHYH(NM_006214.4):c.734G>A (p.R245Q) |
ISCN |
- |
DB-ID |
PHYH_000007 See all 6 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) |
0.00773 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
|