Variant #0000559714 (NC_000016.9:g.88808728T>C, NM_001142864.2:c.263A>G (PIEZO1))
Chromosome |
16 |
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.88808728T>C |
DNA change (hg38) |
g.88742320T>C |
Published as |
PIEZO1(NM_001142864.2):c.263A>G (p.(Asp88Gly)), PIEZO1(NM_001142864.4):c.263A>G (p.D88G) |
ISCN |
- |
DB-ID |
PIEZO1_000177 See all 2 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) |
0.00237 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
|