Variant #0000657985 (NC_000016.9:g.88804736G>A, NM_001142864.2:c.747C>T (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.88804736G>A |
DNA change (hg38) |
g.88738328G>A |
Published as |
PIEZO1(NM_001142864.4):c.747C>T (p.C249=) |
ISCN |
- |
DB-ID |
PIEZO1_000226 |
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) |
4.0E-5 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2020-07-10 15:48:39 +02:00 (CEST) |

Variant on transcripts
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