Variant #0000539525 (NC_000010.10:g.13320306_13320308dup, NM_006214.3:c.1010_1012dup (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.13320306_13320308dup |
DNA change (hg38) |
g.13278306_13278308dup |
Published as |
PHYH(NM_001037537.1):c.710_712dupATC (p.N237_L238insH), PHYH(NM_001037537.2):c.710_712dupATC (p.N237_L238insH), PHYH(NM_006214.4):c.1010_1012dupATC... |
ISCN |
- |
DB-ID |
PHYH_000023 See all 4 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) |
Retrieve |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|