Variant #0000802948 (NC_000007.13:g.135323351G>T, NM_015135.2:c.5312G>T (NUP205))
Chromosome |
7 |
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.135323351G>T |
DNA change (hg38) |
- |
Published as |
NUP205(NM_015135.2):c.5312G>T (p.S1771I) |
ISCN |
- |
DB-ID |
NUP205_000009 |
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) |
0.00225 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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