Variant #0000865148 (NC_000017.10:g.32962058G>A, NM_207313.1:c.1659G>A (TMEM132E))
Chromosome |
17 |
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.32962058G>A |
DNA change (hg38) |
- |
Published as |
TMEM132E(NM_001304438.1):c.1929G>A (p.V643=) |
ISCN |
- |
DB-ID |
TMEM132E_000016 |
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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2022-05-09 16:01:56 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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